LIPO US Equity☆

Item 1A. Risk Factors 25

Item 1B. Unresolved Staff Comments 53

Item 2. Properties 53

Item 3. Legal Proceedings 54

Item 4. Mine Safety Disclosures 54

Item 6. [Reserved] 55

Item 7A. Quantitative and Qualitative Disclosures about Market Risk 64

Item 8. Financial Statements and Supplementary Data 64

Item 9A. Controls and Procedures 64

Item 9B. Other Information 65

Item 9C. Disclosure Regarding Foreign Jurisdictions That Prevent Inspections 65

PART III 66

Item 10. Directors, Executive Officers and Corporate Governance 66

Item 11. Executive Compensation 72

Item 14. Principal Accountant Fees and Services 84

Item 15. Exhibits and Financial Statement Schedules 85

5

pART

i

Item

1. Business

Overview

We

are a clinical-stage biotechnology company that was incorporated under the laws of the State of Delaware in February 2005. We

are focused on developing new drugs by reformulating the active agents in existing generic drugs and optimizing these reformulations

for new applications.

We

believe that our strategy combines many of the cost efficiencies and risk abatements derived from using existing generic drugs

with potential patent protections for our proprietary formulations; this strategy allows us to expedite, protect, and monetize

our product candidates. Additionally, we maintain a therapeutic focus on diseases with significant, unaddressed morbidity and

mortality where no approved drug therapy currently exists. We believe that this focus can potentially help reduce the cost, time

and risk associated with obtaining marketing approval. We have not yet commercialized any products, and we do not expect to generate

revenue from sales of any product candidates for several years.

Our

Lead Product Candidates: LP-10 and LP-310

Consistent

with our strategy, the initial indication that we are currently addressing (via development of our product candidate, which we

have designated as LP-10) is “hemorrhagic cystitis” (“HC”), which is chronic, uncontrolled urinary blood

loss that results from certain chemotherapies (such as alkylating agents) or pelvic radiation therapy (also called “radiation

cystitis”). Many radiation cystitis patients experience severe morbidity (and in some cases, mortality), and currently,

there is no therapy for their condition approved by the FDA, or, to our knowledge, any other regulatory body.

LP-10

is the development name of our reformulation of tacrolimus (an approved generic active agent) specifically optimized for topical

deposition to the internal surface of the urinary bladder lumen using a proprietary drug delivery platform that we have developed

and that we refer to as our metastable liposome drug delivery platform (our “Platform”). We are developing LP-10 and

our Platform to be, to our knowledge, the first drug candidate and drug delivery technology that could be successful in treating

cancer survivors who acquire HC. Our first issued U.S. patent covering LP-10 expires July 11, 2035, unless extended, and our second

issued U.S. patent covering the method of making LP-10 expires November 9, 2034, unless extended. Our issued Australian patent

covering LP-10 expires October 22, 2034. The Canadian patent, issued on August 23, 2022, expires October 22, 2034. We also have

a corresponding patent application pending in the U.S. (U.S.S.N. 17/829,960) and a corresponding allowed patent application pending

in the European Patent Office, which has been allowed, but not yet granted. We also have a pending U.S. patent application on

an improvement to the technology. We have received FDA “orphan drug” designation covering LP-10 and plan to apply

for additional regulatory designations in the event we achieve qualifying results in the current phase 2a clinical trial for LP-10.

The

safety and efficacy of LP-10 was evaluated in a 13-subject, open-label, multi-center, dose-escalation, phase 2a clinical trial

in patients experiencing complications associated with a rare but highly morbid disease called “radiation-induced hemorrhagic

cystitis” or “radiation cystitis.” This phase 2a clinical trial commenced on February 15, 2021, and we reported

the trial’s summary results in the first quarter of 2023. There is currently no FDA approved drug therapy available for

radiation cystitis patients, who are all cancer survivors who received pelvic radiation therapy to treat solid pelvic tumors,

including prostate and ovarian cancers and who are now dealing with therapy-associated complications, including urinary bleeding

(a radiation cystitis symptom). LP-10’s active ingredient, tacrolimus, which has a well-known pharmacology and toxicology,

addresses a reduction (or cessation) of uncontrolled urinary bleeding.

In

a second program, we are developing a product candidate, which we have designated LP-310 and which employs a formulation similar

to LP-10, for the treatment of oral lichen planus (“OLP”). OLP is a chronic, T-cell-mediated, autoimmune oral mucosal

disease, and LP-310 contains tacrolimus which inhibits T-lymphocyte activation. Symptoms of OLP include painful burning sensations,

bleeding and irritation with tooth brushing, painful, thickened patches on the tongue, and discomfort when speaking, chewing or

swallowing. These symptoms frequently cause weight loss, nutritional deficiency, anxiety, depression, and scarring from erosive

lesions. OLP can also be a precursor to cancer, predominately squamous cell carcinoma, with a malignant transformation rate of

approximately one percent.

6

LP-310

is the development name of our oral, liposomal formulation of tacrolimus (the same approved generic active agent in LP-10) specifically

optimized for local delivery to oral mucosa. We believe that our approach of using metastable liposomal tacrolimus as a treatment

for OLP is novel. To date, upon review of relevant FDA public data resources on approved drugs and biologics, we are not aware

of any other liposomal products developed to treat such disease. We have completed a pre-investigational new drug (“IND”)

meeting with the FDA and intend to submit the full IND application to the FDA for LP-310 in the third quarter of 2023. Our issued

U.S. and Australian patents covering LP-310 expire July 11, 2035, October 22, 2034 and October 22, 2034, respectively. The Canadian

patent, issued on August 23, 2022, expires October 22, 2034. We also have a corresponding patent application pending in the U.S.

(U.S.S.N. 17/829,960) and a corresponding allowed patent application pending in the European Patent Office. We also have a pending

U.S. patent application on an improvement to the technology.

Our

Metastable Liposome Drug Delivery Platform

We

have developed a proprietary technology, referred to as our Platform, which is optimized for local hydrophobic drug delivery to

body cavities having endothelial surfaces. Our process employs liposomal technology protected by issued patents in the United

States, Australia and Canada. We also have a corresponding patent application pending in the U.S. (U.S.S.N. 17/829,960) and a

corresponding allowed patent application pending in the European Patent Office. This technology involves direct drug delivery

to the urinary bladder mucosa, and, we believe, has the potential to improve efficacy (by increasing drug concentration at the

site of injury) and to reduce the possibility of side effects (by reducing the drug’s exposure to unrelated organs). The

first body-cavity application for which we intend to utilize our Platform is the urinary bladder, which has been designed to deliver

LP-10. We are also developing an oral cavity product for the treatment of OLP using our Platform (LP-310). We are continuing to

research and develop products for additional body cavities, including the anal-rectal cavity (radiation proctitis) and the esophagus

(eosinophilic esophagitis). We have a pending U.S. patent application on a new embodiment of this technology.

We

predict that our Platform will provide a superior approach for treating inflammatory urinary bladder conditions compared to other

delivery mechanisms and that certain inherent features of the metastable liposomes, combined with our intravesical formulations,

provides our Platform with several advantages over existing bladder drug delivery methodologies in current clinical practice for

inflammatory bladder applications. These advantageous characteristics include the following:

● large payload capacity of hydrophobic agents (10% by mass);

● urothelial affinity, which results in efficient drug transfer;

● low systemic distribution (large particle size);

● reproducible manufacturing and scalability; and

● prior clinical experience utilizing the liposomal delivery vehicle.

The

following table summarizes our therapeutic candidate pipeline and discovery research programs:

Figure 1

7

Our

Strengths

We

believe we are uniquely positioned to employ liposome technology in the development of intravesical treatments for urinary bladder

indications due, in part, to our particular strengths, including:

o our receipt of FDA “orphan drug” designation covering LP-10;

Our

Strategy

We

are, to our knowledge, currently developing the first drug candidate and proprietary drug delivery platform that could be successful

in treating cancer survivors who acquire HC and we intend to apply our proprietary drug delivery technology to the oral mucosa

for the treatment of OLP. Our development programs are designed to address opportunities for capital efficient drug discovery

and development, especially research programs that reposition existing therapeutics for new indications that exploit new formulations.

The key elements of the strategy that we are employing to achieve our goals are:

8

Our product development strategy involves combining intellectual property protection for novel formulations

and indications for approved active pharmaceutical ingredients (“APIs”) with regulatory efficiencies provided by obtaining

FDA designations that make our product candidates eligible for certain incentives that expedite development and review. We believe

that this product development strategy is more capital efficient compared to traditional discovery of a new chemical entity because

the safety and mechanisms of the approved APIs for the novel formulations of our product candidates are better understood and established.

In the United States, approval of API products follows the “505(b)(2) regulatory pathway”; which permits us to rely

on existing research and development (“R&D”) data pertaining to the generic active ingredient. The 505(b)(2) regulatory

pathway often provides an alternate path to FDA approval for new or improved formulations or new uses of previously approved products.

Using a 505(b)(2) new drug application (“NDA”), we expect to reduce the cost, time and risk that would otherwise be

associated with bringing these programs to market. See “Government Regulation Applicable To Our Business – The

505(b)(2) NDA Regulatory Pathway” below for more information.

LP-10

and the Intended Treatment of HC

We

recently completed our phase 2a clinical trial of LP-10 and reported top-line results in January 2023. LP-10 relies on intravesical

vasoconstrictive and anti-inflammatory drug therapy for our intended treatment of HC, a rare and severe consequence of cancer

therapy for which there is currently no approved treatment. HC affects the bladder lining and is caused by the protein-cross-linking

effects of chemotherapy as well as longer-term effects from radiation-induced damage to urothelial tissue. In HC patients, the

urothelial damage results in significant urinary bleeding, inducing the need for blood transfusions. Those cancer patients who

acquire HC suffer from pain and discomfort that accompanies their bleeding. Based on information from the American Cancer Society

as well as published reports on the incidence of HC resulting from either chemo or radiation therapy, we believe there are approximately

72,000 patients annually in the United States who suffer from a severe form of radiation-induced HC and an estimated 60,000 patients

annually with systemic chemotherapy-induced HC. We received “orphan drug” designation from the FDA for the use of

tacrolimus (including LP-10) for the treatment of HC.

We

believe that our approach of using metastable liposomal tacrolimus as a treatment for HC, which has not yet been approved by the

FDA, is novel. To date, we are not aware of any other liposomal products developed for clinical urinary bladder instillation.

The current standard of care for HC patients is limited to measures such as irrigation and cauterization, which seek to reduce

or halt the urinary bleeding of HC but often do not work effectively. There is no approved treatment for HC, and there are currently

no other drug treatments for HC in clinical development of which we are aware. LP-10 is designed to be an acute treatment for

HC to be administered via urinary catheter either at a hospital or doctor’s office within 30 minutes, which would be repeated

daily for a total of four instillations in the same number of days. LP-10 seeks to treat HC via two mechanisms: high local vasoconstriction

and longer-term anti-inflammation.

9

On

December 23, 2019, we received IND approval from the FDA for LP-10, including approval for LP-10’s proposed clinical protocol,

and central investigational review board (“IRB”) approval of our IND-approved clinical protocol, as well as approval

for the investigator’s brochure and patient’s informed consent associated with LP-10. From 2020 to 2022, we signed

clinical trial agreements in connection with eight clinical sites to conduct the dose-escalation, phase 2a clinical trial of LP-10.

We recently completed the phase 2a dose-escalation trial (reporting results in January 2023) and intend to apply for FDA accelerated

approval pathways, including FDA Breakthrough Therapy designation and the design of a pivotal phase 3 clinical trial. If successful,

we believe the results of an LP-10 phase 3 trial could support the submission of an NDA for LP-10 to the FDA through the 505(b)(2)

regulatory pathway and a Marketing Authorization Application (“MAA”) to the EMA in Europe. However, there can be no

assurance that we will obtain such designation from, or be permitted to use such pathway by, the FDA, who is ultimately responsible

for making such determinations.

Background

on HC

HC

is characterized by the presence of sustained hematuria and lower urinary tract symptoms in the absence of active tumor and other

conditions or infections that cause excessive bleeding, (Gorzynska et al. 2005). Urologic adverse events caused by HC include

frequency, dysuria, urgency, nocturia, suprapubic pain, bladder infection, fatigue and both microscopic and gross hematuria.

Bleeding

from HC ranges from non-visible (or microscopic) hematuria to gross (visible) hematuria with clots (Decker et al. 2009). Moderately

severe cases of HC involve massive bleeding and clot formation. Severe HC is a challenging condition to treat and may give rise

to serious complications, leading to prolonged hospitalization and/or mortality (Decker et al. 2009; Mukhtar and Woodhouse 2010)

and HC cases resulting from chemotherapy are reported to have a mortality rate approaching 4% (Rastinehad et al. 2007). Even mild

cases of HC can cause disabling symptoms (e.g., frequency, urgency and pelvic pain, often localized to the bladder or urethra)

(Payne et al. 2013). A standardized grading system (Droller et al. 1982) to classify the severity of HC has been proposed, which

is shown in Figure 2 below:

Figure

2

HC

can be classified as early- or late-onset (Zwaans et al. 2016). HC can also develop weeks to months after treatment in 20%–25%

of patients who receive high doses of cyclophosphamide. The effects of radiation-induced HC may be acute or delayed, occurring

long after radiation treatment has ended, from two months to 15 years later (Zwaans et al. 2018; Manikandan et al. 2010).

10

Prevalence

At

the suggestion of the FDA’s Office of Orphan Products Development, we have measured annual cyclophosphamide and ifosphamide

use in a large commercial database for private health plans between 2008 and 2010 and, based on guidance from the FDA, applied

a 40% rate of HC in such patient database. The information from the database, combined with the FDA’s recommended guidance,

results in a prevalence of consequential HC to potentially reach 60,000 new cases per year in the United States. This methodology

implicitly assumes that the prevalence of use observed in private health plans (including Medicare beneficiaries enrolled in private

plans) is generalizable to the nation as a whole, and such figure represents our conservative estimate of the number of new cases

per year after applying the FDA’s recommended 40% rate to the figures in such patient database. HC resulting from pelvic

radiation therapy (occurring in the prostate, rectum and uterine corpus) is less common than HC resulting from chemotherapy and

is believed to be proportional to the incidence of the “primary neoplasia” (the original malignancy). Such incidence

of HC is based on a combined estimate of the incidence of both chemotherapy-induced HC and radiation-induced HC from (i) peer-reviewed

literature estimating the proportion of cyclophosphamide and ifosphamide recipients that acquire chemotherapy-induced HC after

undergoing chemotherapy, as applied to a national chemotherapy incidence measurement study, and (ii) peer-reviewed literature

containing estimates of the proportion of cancers treated with pelvic radiation therapy and the number of years patients survive

post-radiation therapy, in addition to pelvic cancer incidence estimates publicly available from sources such as the American

Cancer Society. According to the American Cancer Society publication Cancer Facts & Figures 2022 (available

at: https://www.cancer.org/content/dam/cancer-org/research/cancer-facts-and-statistics/annual-cancer-facts-and-figures/2022/2022-cancer-facts-and-figures.pdf),

there are 268,490 new cases of prostate cancer in the U.S. each year, 151,030 new cases of rectum and colon cancer in the U.S.

each year, and 65,950 cases new cases of uterine corpus cancer in the U.S. each year. Based, in part, on this data, we estimate

the U.S. incidence of HC to be in the range of approximately 100,000 to 200,000 cases per year.

Existing

Treatment Options

There

is currently no standard therapy available for patients with HC, and there are no guidelines available on how HC should be optimally

managed. Current HC treatments are regarded as ineffective, risky, or both. Such treatments include general medical management

(e.g., estrogens, pentosan-polysulfate, and hyperbaric oxygen (“HBO”)), instillation therapy (e.g., aminocaproic-acid,

alum, silver-nitrate, formalin, and fibrin glue), embolization and surgery (e.g., coagulation and cystectomy). The moderately

severe cases of HC involve massive bleeding as well as clot formations that require evacuation. The most severe cases require

surgical intervention (e.g., urinary diversion or cystectomy) (Sant 2002; Perez-Brayfield and Kirsch 2009). In addition, we believe

current treatments pose significant patient risk: interventional fulguration of bleeding sites rarely works and exposes sick,

frail patients to surgical risks; treatment with aminocaprotic acid often leads to dangerous clots; treatment with silver nitrate

can cause bladder perforation or kidney failure; and treatment with formalin significantly reduces bladder functionality and causes

excruciating pain (Vicente, Rios et al. 1990).

HBO

treatments for HC may decrease and prevent the risk of bleeding but cannot treat ongoing bleeding, in part because therapy takes

up to 40 sessions over a period of two to three months. Cystectomy causes significant morbidity and is generally an option of

last resort; in some cases where cystectomy is conducted, old and/or frail patients can bleed to death. There are no other products

in development of which we are aware that are indicated for the treatment of HC. Should LP-10 ultimately receive FDA market approval,

we believe it will address this unmet medical need and provide a benefit over existing products while fitting into the existing

treatment algorithm as a treatment for refractory HC.

LP-10’s

Mechanisms of Action – Tacrolimus

LP-10’s

API tacrolimus has been approved by the FDA for systemic use for inhibiting transplant rejection and as topical ointment for moderate

to severe atopic dermatitis. Tacrolimus acts by inhibition of IL-2-dependent T-cell activation and has a direct inhibitory effect

on cell-mediated immunity (Kino et al., 1987; Tamura et al., 2002). Tacrolimus prolongs the survival of the host and transplanted

graft in animal transplant models of liver, kidney, heart, bone marrow, small bowel and pancreas, lung and trachea, skin, cornea

and limb. In animals, tacrolimus has been demonstrated to suppress some humoral immunity and, to a greater extent, cell-mediated

reactions such as allograft rejection, delayed type hypersensitivity, collagen-induced arthritis, experimental allergic encephalomyelitis

and graft versus host disease. Tacrolimus inhibits T-lymphocyte activation, though the exact mechanism is not known. Experimental

evidence suggests that tacrolimus binds to an intracellular protein named FKBP-12. A complex molecule comprising tacrolimus-FKBP-12,

calcium, calmodulin and calcineurin is formed and the phosphatase activity of calcineurin is inhibited. This effect may prevent

the dephosphorylation and translocation of the nuclear factor of activated T-cells, a nuclear component thought to initiate gene

transcription for the formation of lymphokines (such as interleukin-2, gamma interferon). The net result is the inhibition of

T-lymphocyte activation (i.e., immunosuppression).

11

The

urothelium is the primary site of tissue damage in the general pathophysiology of cystitis (Erdogan et al. 2002). Recent studies

have highlighted the overexpression of genes related to immune and inflammatory responses, including activation of CD4+ T-helper

type-1-related chemokines in general cystitis (Trompeter et al. 2002; Almawi and Melemedjian 2000). Expression of chemokines precedes

infiltration of immune cells and elevation of chemokines is an established signature of the inflammatory phenotype in bladder

pain. Many of the symptoms of HC are related to inflammation of urothelial tissues. We believe that our application of the liposomal

tacrolimus could potentially have a two-fold effect of (i) inhibiting calcineurin and the related response, and (ii) causing acute

arteriole vasoconstriction to suppress HC (see Figure 2 above). Calcineurin inhibition is the well-known tacrolimus intracellular

signal transduction mechanism that impairs the ability of certain immune cells to activate, and tacrolimus’ vasoconstrictive

properties are referenced, for example, in section “5.7 Nephrotoxicity” of the Label (prescribing information) associated

with the “PROGRAF® (tacrolimus) injection (for intravenous use) Initial U.S. Approval: 1994.”

Non-Clinical

Study Results Involving Intravesical Tacrolimus

The

following is a summary of non-clinical studies conducted with rats and dogs that were sponsored by the Company or conducted in

collaboration with Company scientists. Results from animal studies are not always predictive of results of subsequent human clinical

trials:

Effect

of intravesical-tacrolimus on chemotherapy-induced HC

In

September 2010, the effect of intravesical-tacrolimus was examined in a rat model for chemotherapy-induced, intraperitoneal injection

of cyclophosphamide (200 mg/kg; i.p.) HC. This study demonstrated that cyclophosphamide-induced hyperactivity (i.e., decrease

in inter-contraction interval) was suppressed in rats with intravesical LP-10 treatment but not in the rat groups left untreated

(sham) or treated with empty liposomes (vehicle control) (Chuang et al. 2010). This result indicates that liposomal tacrolimus

may mitigate cyclophosphamide injury in an animal model (Neurology and Urodynamics 30:421-427 (2011)).

Effect

of intravesical-tacrolimus on radiation-induced HC

In

October 2012, the efficacy of intravesical-tacrolimus was also examined in a rat model for radiation-induced HC. A 40 Gy radiation

dose induced statistically significant reductions in the intermicturition interval recorded during metabolic urination patterns.

Irradiated rats were randomly assigned to receive a single instillation of saline or intravesical-tacrolimus. Intravesical-tacrolimus

increased the post-irradiation intermicturition intervals (p <0.001). Rat bladders that were harvested six weeks after the

40 Gy irradiation doses and two weeks after saline instillation showed edematous changes accompanying infiltration of inflammatory

cells and hyperplastic urothelial changes. In contrast, bladder from group treated with intravesical-tacrolimus shows minimal

edematous change, consistent with the hypothesis that the intravesical-tacrolimus had an anti-inflammatory effect (J. of Urology

194, 578-584 (2015)).

Pharmacokinetics

of sphingomyelin formulated tacrolimus

A

2013 study examined levels of tacrolimus in blood, urine and bladder tissue following a single dose of liposome formulated tacrolimus

instilled in the bladder of rats under anesthesia as compared to intravesical instillation of tacrolimus or intraperitoneal injection

of tacrolimus in other rat groups. The tacrolimus dose was constant in all formulations at 200g/ml. At different times, blood,

urine and bladder samples were collected. Tacrolimus levels in samples were analyzed using microparticle enzyme immunoassay. The

area under curve (“AUC”) of liposome tacrolimus in serum at 0 to 24 hours was significantly lower than that of tacrolimus

instillation or injection. Non-compartmental pharmacokinetic data analysis revealed maximum concentration of liposomal tacrolimus

and tacrolimus in blood and urine at one and at two hours, respectively. Urine AUC (0–24 hours) after intravesical administration

was significantly higher than in the intraperitoneal group (p < 0.05). Bladder tacrolimus AUC (0–24 hours) did not differ

significantly between the groups. Single dose pharmacokinetics revealed that bladder instillation of liposome tacrolimus significantly

decreased systemic exposure to instilled tacrolimus. This appears to indicate that a reduction in systemic exposure helps to limit

the potential side effects of the tacrolimus by concentrating the dose to only one organ (J. of Urology Vol. 189, 1553-1558 (2013)).

12

LP-10

Toxicology Studies

In

2018, we completed chronic toxicology studies in rats and dogs, which were the two species of animals that we agreed to study

in the course of our pre-IND communications with the FDA. The completion of such studies is normally required prior to requesting

IND approval. The in-life phase of the toxicology rat study was performed between February and March 2018 and the in-life phase

of the dog toxicology study was performed in March 2018. Such studies were company-sponsored and conducted by qualified vendors

specializing in good laboratory practice in-vivo toxicology studies. The animals in such 2018 studies were assessed for morbidity,

mortality, clinical observations and weekly body weight. Full sets of standard tissues, including urinary tract tissues, were

collected and weighed and histopathology evaluations were conducted from all such animals. The studies concluded that no significant

local and systemic toxicity resulted from the administration of LP-10 by intravesical instillation in either rats or dogs.

LP-10’s

Addressable Market

LP-10

has been designed for the approximately one million cancer survivors in the United States today who have had pelvic radiation

therapy and are at risk for HC. Based on the managed care database study that we sponsored in 2012 as part of our approved request

for FDA “orphan drug” designation of tacrolimus for HC, approximately 72,000 of these patients annually experience

severe chronic bladder bleeding that is often fatal. LP-10 has been developed to address this form of bleeding, as well as bladder

bleeding associated with breast cancer patients who are taking systemic cyclophosphamide or ifosfamide, leading to chemotherapy-related

cystitis experienced by an estimated 60,000 patients annually in the United States, inferring an addressable market in excess

of 120,000 patients annually.

Figure

3

(1)

American Cancer Society Cancer Facts and Figures 2022, (2) derived from a Company-sponsored study, (3) based on the Company’s

40% estimate, (4) American Cancer Society Cancer Treatment and Survivorship Fact and Figures 2019-2021, (5) based on the Company’s

30% estimate (6) 8% estimate, (7) based on the Company’s estimate, (8) $20,000 average revenue per each of an estimated

60,000 patients treated per year.

Figure

3 above illustrates the potential sources of revenue for LP-10. LP-10 is not currently approved for any indication; however, if

clinical development is successful and we receive marketing approval for LP-10, we estimate the average LP-10 price to exceed

$20,000 per patient-year domestically. This estimate is based on costs of HBO therapy, which is an option for patients with mild

cases. HBO therapy can cost approximately $15,000 for a course of 30 sessions. Our price estimate also includes the potential

for associated reductions in direct medical expenditures, especially for severe cases. We estimate the peak demand, at this price,

to be, approximately 60,000 patients annually, which represents an approximate 50% market penetration in the U.S. Based on such

price and demand estimates, we believe there is potential to receive up to $1.2 billion in annual gross revenue.

13

Our

Lead Drug Candidate, LP-10, and Our Product Pipeline

Five

fundamental aspects of our LP-10 drug candidate make it an excellent fit for our strategy (see Figure 4 below). First, our API

has a well-known mechanism of action. Second, published non-clinical studies involving animals, which are described above, demonstrate

the potential for significant efficacy in our intended indication and route of administration. Third, we are fortunate to have

had a successful human experience with intravesical tacrolimus (Dave et. al. Int Urol Nephrol 2015). Fourth, we believe we can

take advantage of accelerated regulatory approval pathways for LP-10; we have already received “orphan drug” designation

from the FDA that grants us product exclusivity, and we plan to apply for designations under one or more of the FDA’s expedited

development and review programs. Fifth, we believe that the revenue potential for LP-10 could be significant. We believe our focus

on capital-efficient drug development provides us with additional opportunities as we evaluate potential drug candidates for other

rare diseases, especially those associated with locally delivering drugs to body cavities. When evaluating opportunities, we ensure

that both the indication as well as the regulatory pathway are conducive to capital-efficient

drug development. Our product candidate pipeline includes product candidates that could treat OLP (LP-310). Most recently, on

April 8, 2021, we received the FDA’s response to our February 8, 2021 pre-IND meeting request and docket regarding formulation,

non-clinical toxicology and proposed clinical protocol for LP-310, providing clarity regarding our requirements for IND submission.

We believe that our current product candidate pipeline could enable us to apply our drug delivery technology (our Platform) for

multiple types of severe, rare diseases, and in the future, could enable us to address additional broader indications associated

with endothelial inflammation. Local delivery often allows us to avert known risk factors by only locally applying the effective

dose.

Figure

4

We

are currently evaluating several potential product candidates for additional indications (including radiation proctitis and eosinophilic

esophagitis).

LP-10’s

Regulatory Status

In 2019, we completed the required manufacturing and toxicology program to submit an IND request to the

FDA to begin testing LP-10 in human subjects. We submitted the IND request in September 2019 and received approval from the FDA

within 30 days of submission to begin a clinical study involving LP-10. In December 2019, we received an advice letter from the

FDA recommending several modifications to our proposed clinical protocol for LP-10, which we accommodated. We also submitted and

received approval from the FDA for the trial’s associated investigator brochure and the proposed documentation of patient

consent. Both of these documents, in addition to the clinical protocol, were submitted to Adverra, our central IRB, and we subsequently

received IRB approval to conduct our clinical trial. In February 2020, the first patient was dosed in LP-10’s FDA phase 2a

open-label, dose-escalation clinical trial for patients experiencing moderate to severe HC, which is intended to demonstrate proof-of-concept

in humans. We reported summary results from LP-10’s phase 2a clinical trial in January 2023.

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LP-10’s

FDA “Orphan Drug” Designation Status

In

2010, we submitted a request to the FDA for “orphan drug” designation covering LP-10 and subsequently received approval

for such designation in July 2012. This provides us with marketing exclusivity and permits us to benefit from shorter FDA review

periods and reduced regulatory fees for LP-10. We intend to apply for similar “orphan drug” designations in additional

jurisdictions, including Europe and Japan, as well as additional regulatory classifications, such as the FDA’s Breakthrough

Therapy and Fast Track designations, in the United States. We expect that any designations that we have received, or may in the

future receive, will confer additional advantages during LP-10’s development. However, there can be no assurance that we

will obtain such designations from the FDA, who is ultimately responsible for making such determinations.

LP-10’s

Clinical Status

Our multi-center, open-label dose-escalation phase 2a LP-10 clinical trial involved a total of thirteen

subjects who received tacrolimus doses in one or two instillations of 2, 4 or 8mg via a pre-liposomal lyophilate reconstituted

in 40 milliliters of sterile water. Subjects were cancer survivors with a history of pelvic radiotherapy who developed moderate

to severe HC refractory to conventional therapy. The study was IRB-approved at nine clinical sites within the FDA’s jurisdiction.

Four subjects were enrolled in the 2mg group, four subjects were enrolled in the 4mg group, and five subjects

were enrolled in the 8mg group. All subjects were male, with a median age of 67 years. Nine of the thirteen subjects had a history

of prostate cancer and had been previously treated with external beam radiation. Two of the thirteen subjects had a history of

lymphoma previously treated with radiation, and two had a history of bladder cancer previously treated with radiation.

The last subject of the LP-10 phase 2a study completed the last visit in October 2022. We reported top-line

data from this trial in January 2023. All twenty-three LP-10 instillations in the 2mg, 4 mg and 8mg groups were well-tolerated

by all thirteen subjects without related adverse events or elevated blood tacrolimus levels. For multiple subjects, hematuria

and urinary symptoms improved, and cystoscopic bleeding and ulceration sites decreased. There was a complete response in three

of the subjects, a partial response in seven of the subjects and no response in three of the subjects. We believe that such data

and instillation safety findings indicate LP-10’s tolerability in HC patients and evidence LP-10’s potential use for

the treatment of HC.

LP-310

and the Intended Treatment of OLP

LP-310

is currently in pre-clinical development. LP-310 uses immunosuppressive and anti-inflammatory drug therapy to treat OLP, which

is a chronic immune-mediated mucosal disease characterized by ulcerative lesions in the oral cavity. To date, upon review

of relevant FDA public data resources on approved drugs and biologics, we are not aware of any other liposomal products developed

to treat OLP. Patients are currently treated with off-label steroids for managing painful, erosive or ulcerative lesions. Yet,

there are virtually no steroids formulated for topical drug delivery to lesions in the mouth. For severe and difficult-to-treat

lesions, systemic steroids, and other immunosuppressive agents (e.g., hydroxychloroquin) are often needed, even though OLP is

localized. Creams, gels and ointments do not adhere to oral mucosa and are easily swallowed, while mouthwashes and steroid inhalers

have extremely short contact time with lesions. For severe and difficult-to-treat lesions, systemic steroids are often needed,

even though OLP is localized. As a result, we believe there is great unmet medical need for this disease.

We

believe that our approach of using metastable liposomal tacrolimus as a treatment for OLP, which has not yet been approved by

the FDA, is novel. Tacrolimus has been used as an off-label oral treatment of OLP and it has been shown to be effective based

on systematic review and meta-analysis (Sun et al., 2019), which we believe is indicative of a rationale for using tacrolimus

to treat OLP. Twenty-one trials involving 965 patients were included in this meta-analysis that concluded, in part, that

treatment with tacrolimus may be an alternative approach when OLP does not respond to the standard protocols.

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Background

on OLP

OLP

is a chronic T-cell-mediated mucosal disease that affects more than 1% of the global population, or more than 6 million people

in the U.S. and Europe, according to González-Moles et. al., Oral Diseases 27(4):813-828 May 2021, “Worldwide

prevalence of oral lichen planus: A systematic review and meta-analysis.” OLP is generally divided into three clinical subtypes:

reticular, atrophic or erythematous, and erosive and/or ulcerative. Although lichen planus can be found on other areas of the

body, such as with cutaneous lichen planus (“LP”), OLP has a chronic course, with little chance for spontaneous resolution,

and most therapies that are currently available are palliative rather than curative. Based on peer-reviewed medical literature,

OLP has a prevalence ranging from 1-2%, and females twice as likely as men to have the disease. The age on onset is generally

between 30-60 years. Although cutaneous LP is associated with approximately 15% of OLP cases, OLP is associated with approximately

75% of patients with cutaneous LP.

Symptoms

vary, but the disease is typically characterized by white reticular changes, erythema and painful ulcerative lesions in the oral

cavity, accompanied by inflammation and severe pain. The precise cause is unknown, although an autoreactive immune process is

suspected by most experts in the field. OLP is most frequently located bilaterally on the buccal mucosa (the inside lining of

the cheeks and floor of the mouth), but can also appear on the tongue, palatal mucosa, gingiva and lips. Because of the long-lasting

nature of the disease and painful symptoms, which can be spontaneous or triggered by acidic, crunchy and spicy food, patients

require ongoing care and monitoring. Patients with OLP also have an approximately 1% likelihood of being diagnosed with oral cancer

as a result of OLP (between 0.4% to 5% over a 20-year period, with an annual rate between 0.2% to 0.5%), making early detection

and treatment imperative.

Some

cases of OLP are caused by a hypersensitivity reaction to mercury and formaldehyde or medications such as ACE inhibitors, thiazide

diuretics, beta blockers, gold salts, sulfasalazine, sulfonylureas and penicillamine. The new biologic agents such as TNF alpha

inhibitors may also cause lichen planus-like eruptions. Patients with hypothyroidism, including Hashimoto thyroiditis, also develop

OLP and it is unclear whether it is thyroid disease that predisposes an individual to OLP, or whether the drugs used to treat

such disease also cause OLP. Hepatitis C virus infection has also been associated with the development of OLP in southern European

countries. As mentioned above, we are not aware of any approved treatments for OLP and we do not believe that current treatments

are sufficiently effective.

LP-310’s

Mechanisms of Action

LP-310

contains the API tacrolimus, like LP-10. Recent studies have highlighted that OLP pathophysiology is initiated by cellular-mediated

immunity, most importantly, the increased production of T-helper 1(Th1) cytokines (Chamani et al., 2015). The oral mucosa

is the primary site of tissue damage in the pathophysiology of OLP (Alrashdan et al., 2016). For a discussion of the tacrolimus

API, on which LP-310 relies for its delivery to the oral cavity, and the effect tacrolimus has on T-lymphocyte activation, see

“– LP-10’s Mechanisms of Action – Tacrolimus” above. We believe that our application of the

liposomal tacrolimus to the oral cavity to address OLP could exploit this mechanism with a high local and low systemic distribution.

Planned

Non-Clinical Studies Involving LP-310

The

FDA has recommended small and large animal local and systemic toxicology studies as part of the IND package for HC. Based on our

experience working with the FDA to develop LP-10 for HC, we predict that LP-310 studies would be conducted initially as non-clinical,

in-vivo toxicology studies on male and female rats and dogs. At this time, no such studies have been conducted or are planned.

LP-310’s

Addressable Market

LP-310 is not currently approved for any indication; however, if clinical development is successful and

we receive marketing approval for LP-310, based upon the economics of existing oral cavity drug products, we project that the treatment

of OLP will cost approximately $4,000 annually per patient. Most OLP patients are treated by dentists, who are relatively accessible

compared to other medical specialists (in the United States there are approximately 200,000 dentists and ear, nose and throat physicians).

Currently, dentists routinely recommend and prescribe instill agents as oral rinses and the procedure is simple and easy to teach.

Given the absence of FDA approved treatment of OLP, we estimate revenue of approximately $4,000 per course of therapy, resulting

in a total addressable market that exceeds $980 million. These estimates are based on the prices of other brand intravesical products

as well as our preliminary estimates of the potential for reduction in medical expenditures associated with intractable cases.

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LP-310’s

Regulatory Status

On

April 8, 2021, we successfully completed a pre-IND meeting to confirm the specific IND manufacturing, analytical, toxicology requirements

for LP-310 as an oral rinse for the treatment of OLP.

Facility

We

have approximately 2,000 square feet of combined laboratory, office and warehouse space at our principal executive offices that

we use in our research and development efforts. The lease for our principal executive offices has a five-year term that ends on

May 31, 2024, and the lease provides us with an option to extend the term for an additional five years.

We believe our Facility contains all of the various components necessary to support our research, and

it includes a current good manufacturing practices (“cGMP”)-capable manufacturing capability with a dedicated pilot-scale

manufacturing. The space is divided into a production area and office space, with the production area subdivided into a clean space

(Class 10,000) and sterile space (Class 100 (ISO class 5) clean room). Our Facility includes a pre-fabricated soft-wall, 6’x10’

class-100 clean room for aseptic formulation.

We maintain an internal LP-10 pilot manufacturing facility. We plan to file for an NDA utilizing the 505(b)(2)

regulatory pathway for LP-10, which, if approved, may rapidly increase our manufacturing compliance needs. Even if we are able

to pursue the 505(b)(2) regulatory pathway strategy, however, there is no assurance that we will be successful developing and/or

commercializing LP-10 in a rapid or accelerated manner.

We

are in a continuous process of complying with increasing regulatory requirements as the development of LP-10 progresses. Currently,

our manufacturing process primarily involves facility-dependent sterility protocols surrounding a five-step batch process. The

simplicity of our process provides a strong incentive to continue investing internally in manufacturing compliance.

Compliance with stage-appropriate cGMPs is a prerequisite for FDA approval of a drug product for use in

a clinical trial. cGMP regulations increase as a product candidate enters each subsequent clinical trial phase and as the scope

of a proposed trial increases. Compliance with all cGMP regulations is a requirement for NDA approval and commercialization of

LP-10. We expect to increase the cGMP manufacturing capabilities at our Facility to ensure full-scale compliant production of LP-10.

We

believe that our manufacturing program will be able to support any future clinical trials involving LP-10. We currently lease

industrial space used for cGMP manufacturing and analytical support. The space includes a non-porous epoxy floor, ideally suited

for sterile environments, such as those used in hospital surgical rooms and sterile processing facilities. We have completed initial

characterization and quality control release testing to confirm consistency of production of LP-10. Any applicable revised information

and data will be provided to the FDA as part of an amended Chemistry, Manufacturing and Controls (“CMC”) section of

the IND application prior to and in conjunction with use in any subsequent clinical trial.

Our

Analytical Laboratory, Equipment & Supplies

Our

current preparatory and biochemical/biophysical analysis capabilities include: ultra-centrifugation, high performance liquid chromatography

(“HPLC”); differential scanning calorimetry (“DSC”); gas chromatography (“GC”); cross-polarization

microscopy; fluorescent microscopy; near-infra-red imaging; and particle size analysis. In addition to the analytical equipment

and sterile cleanroom, our Facility it contains a laminar flow hood for sterile procedures outside of the cleanroom, two Labconco

lyophylizers (each with a 50-vile capacity), multiple incubators, a laboratory oven, an autoclave, various mass balances, vortexes,

a heat stage for our optical microscope, various freezers and refrigerators, chemical and flammable storage cabinets, sterile

disposables (including clothing, materials and vials), and raw materials, including APIs and lipids.

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Suppliers

We

obtain our raw material supply of LP-10 from multiple vendors who have a drug master file with the FDA. It is supplied as a white,

lyophilized powder (a pre-liposomal lyophilate) formulated from sphingomyelin phospholipids, and tacrolimus. One vial of LP-10

drug product contains 80mg of tacrolimus and sphingomyelin (10% tacrolimus by weight) and is supplied to a clinic as a powder

to be reconstituted with sterile water for injection prior to instillation. Quality control samples from each batch would be submitted

for release testing according to established product specifications for identity and purity, residual solvent quantification,

sterility assurance, and bacterial endotoxins.

Intellectual

Property

Protection of our intellectual property is an important part of our business. On May 5, 2020, we were

issued U.S. patent number 10,639,278 (the “278 Patent”) from the United States Patent and Trademark Office (“USPTO”),

which does not expire until July 11, 2035. On June 14, 2022, we were issued U.S. patent number 11,357,725 (the “725 Patent”),

which does not expire until November 9, 2034. Further, on May 28, 2020, we were issued one patent in Australia (No. 2014340137)

(the “Australia Patent”), which does not expire until October 22, 2034. On August 23, 2022, we were issued on patent

in Canada (No. 2,927,356) (the “Canadian Patent”), which does not expire until October 22, 2034. Each of the aforementioned

patents cover aspects of our Platform technology relating to uses for delivering hydrophobic therapeutic, prophylactic or diagnostic

agents to the body cavities, including LP-10 and LP-310, as well as methods of making formulations for delivering such hydrophobic

agents. We are also actively prosecuting corresponding utility patent applications in the U.S. and in Europe, the latter of which

has been allowed, but not yet granted. We intend to seek additional patent applications in the U.S. as well as in other jurisdictions,

such as Europe, for our other proprietary technologies relating to intravesical immunoglobulin delivery and any future discoveries

that we deem appropriate to protect. A U.S. patent application on the intravesical immunoglobulin delivery formulation is pending.

In

addition to patents, we rely on trade secrets and know-how relating to our Platform technology and the product candidates we are

developing using our Platform to develop and maintain our competitive position. However, trade secrets can be difficult to protect.

We intend to protect our proprietary technology and processes, and maintain ownership of certain technologies, in part, through

licenses as well as confidentiality agreements and invention assignment agreements with our employees, consultants and commercial

partners.

Government

Regulation Applicable to Our Business

In

the United States, the FDA regulates drug products, including liposomally delivered products, under the FDCA, the Public Health

Service Act (the “PHSA”), and regulations and guidance implementing these laws. The FDCA, PHSA and their corresponding

regulations govern, among other things, the testing, manufacturing, safety, efficacy, labeling, packaging, storage, record keeping,

distribution, reporting, advertising and other promotional practices involving drug products. Applications to the FDA are required

before conducting human clinical testing of drug products. FDA approval also must be obtained before marketing of drug products.

The process of obtaining regulatory approvals and the subsequent compliance with appropriate federal, state, local and foreign

statutes and regulations require the expenditure of substantial time and financial resources and we may not be able to obtain

the required regulatory approvals to successfully develop and commercialize our product candidates, including LP-10.

18

U.S.

Drug Development Process

The

FDA must approve a product candidate before it may be legally marketed in the United States. The process required by the FDA before

a drug product candidate may be marketed in the United States generally involves the following:

● review of the product by an FDA advisory committee, if applicable;

● payment of user fees and FDA review and approval, or licensure, of the NDA.

Before

testing any drug product candidate in humans, including a liposomal intravesical product candidate, the product candidate must

undergo preclinical testing. Preclinical tests, also referred to as nonclinical studies, include laboratory evaluations of product

chemistry, toxicity and formulation, as well as in vivo studies to assess the potential safety and activity of the product candidate

and to establish a rationale for therapeutic use. The conduct of the preclinical tests must comply with federal regulations and

requirements including GLPs.

Concurrent

with clinical trials, companies usually must complete some long-term preclinical testing, such as animal studies of reproductive

adverse events and carcinogenicity, and must also develop additional information about the chemistry and physical characteristics

of the drug and finalize a process for manufacturing the drug in commercial quantities in accordance with cGMP requirements. The

manufacturing process must be capable of consistently producing quality batches of the drug candidate and, among other things,

the manufacturer must develop methods for testing the identity, strength, quality and purity of the final drug product. Additionally,

appropriate packaging must be selected and tested and stability studies must be conducted to demonstrate that the drug candidate

does not undergo unacceptable deterioration over its shelf life.

The

clinical trial sponsor must submit the results of the preclinical tests, together with manufacturing information, analytical data,

any available clinical data or literature and a proposed clinical protocol, to the FDA as part of an IND. Some preclinical testing

may continue even after the IND is submitted. The IND automatically becomes effective 30 days after receipt by the FDA, unless

the FDA places the clinical trial on a clinical hold. In such a case, the IND sponsor and the FDA must resolve any outstanding

concerns before the clinical trial can begin. The FDA also may impose clinical holds on a drug product candidate at any time before

or during clinical trials due to safety concerns or non-compliance. If the FDA imposes a clinical hold, trials may not recommence

without FDA authorization and then only under terms authorized by the FDA.

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Human

Clinical Trials Under an IND

Clinical

trials involve the administration of the drug product candidate to healthy volunteers or patients under the supervision of qualified

investigators which generally are physicians not employed by, or under, the control of the trial sponsor. Clinical trials are

conducted under written study protocols detailing, among other things, the objectives of the clinical trial, dosing procedures,

subject selection and exclusion criteria and the parameters to be used to monitor subject safety, including stopping rules that

assure a clinical trial will be stopped if certain adverse events should occur. Each protocol and any amendments to the protocol

must be submitted to the FDA as part of the IND. An IND automatically becomes effective 30 days after receipt by the FDA, unless

before that time the FDA raises concerns or questions related to a proposed clinical trial and places the trial on clinical hold,

including concerns that human research subjects will be exposed to unreasonable health risks. In such a case, the IND sponsor

and the FDA must resolve any outstanding concerns before the clinical trial can begin. Accordingly, submission of an IND may or

may not result in the FDA allowing clinical trials to commence. Clinical trials must be conducted and monitored in accordance