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JSP191 Antibody Targeting Conditioning in SCID Patients

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NCT02963064

Sponsored by Jasper Therapeutics, Inc. (industry) · JSPR — their whole pipeline →.

Phase
Phase 1/2
Status
Terminated
Study type
Interventional
Design
Na · None · Treatment
Enrollment
23actual
Sites
9
Country
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

Why the sponsor stopped it

Sponsor Decision - terminated due to changes in company priorities and not related to safety concerns.

As filed on the registry record, in the sponsor's own words.

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2017-03-20actualWhen the study began enrolling
Primary completion2025-07-07actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2025-07-07actualThe whole study's end, after follow-up
First posted2016-11-15estimatedWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-07-28actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • SCID

Intervention

  • Biological: Humanized anti-CD117 Monoclonal Antibody (JSP191)

Primary outcomes

what the primary-completion date above is the date OF
Phase 1: Safety and tolerability of JSP191 as conditioning therapy in SCID patients undergoing HCT: adverse events
measured Up to 5 years post Donor Cell Transplant (28 days dose limiting toxicity period)
Phase 2: Efficacy of JSP191 as conditioning therapy in SCID patients
measured Up to 24 weeks post Donor Cell Transplant
Phase 2: Efficacy of JSP191 as conditioning therapy in SCID patients
measured Weeks 36-104 post Donor Cell Transplant

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