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A Phase 1 Clinical Study of NXP900 in Subjects With Advanced Cancers

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NCT05873686 · readout ≤ 224 d

Sponsored by Nuvectis Pharma, Inc. (industry) · NVCT — their whole pipeline →.

Phase
Phase 1
Status
Recruiting
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
140estimated
Sites
15
Countries
United Kingdom, United States

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2023-10-26actualWhen the study began enrolling
Primary completionMar 2027estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionJul 2027estimatedThe whole study's end, after follow-up
First posted2023-05-24actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-07-09actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Advanced Solid Tumor
  • NSCLC (Non-small Cell Lung Cancer)
  • Renal Cancer
  • Mesothelioma
  • Non-Small Cell Squamous Lung Cancer
  • Non-small Cell Lung Adenocarcinoma

Intervention

  • Drug: NXP900

Primary outcomes

what the primary-completion date above is the date OF
Number of patients with treatment related adverse events and/or clinical laboratory abnormalities
measured Up to 30 days post treatment
Part A: Number of patients who experience Dose Limiting Toxicities (DLT) as defined in the protocol
measured Day 28
Part B: Objective response rate (ORR)
measured Up to 24 months
Part B: Duration of Response (DoR)
measured Up to 24 months
Part B: Disease Control Rate (DCR)
measured Up to 24 months

Publications

Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.

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