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NCT07650357 · ClinicalTrials.gov registry record · Phase 1

A Study of CLSP 5282 in HLA-A*03:01 Positive Adult Patients With Solid Tumors (SENTINEL-101)

A Phase 1 study, sponsored by Clasp Therapeutics.

Not yet
Registry status
Phase 1
Development phase
140
Enrollment target

NCT07650357: Clinical Trial Phase 1 study, sponsored by Clasp Therapeutics.

NCT07650357 is a Phase 1 study that has not yet begun recruiting, run by Clasp Therapeutics. The registered enrollment target is 140 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (133% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07650357, a Phase 1 study, has not yet begun recruiting, sponsored by Clasp Therapeutics.

NOT YET RECRUITING
Registry status
Phase 1
Development phase
140 participants
Enrollment target

Study Summary

Phase 1, open-label, multicenter study to evaluate the safety, tolerability, PK, PD, and preliminary clinical activity of CLSP 5282 when administered to HLA A\*03:01-positive adult patients with advanced solid tumors that harbor the KRas G12V mutation.

Primary Outcome

To characterize the safety and tolerability of CLSP-5282 and to determine the maximum tolerated dose (MTD) and/or recommended dose(s) for expansion (RDE\[s\]).

Interventions

  • DRUG CLSP-5282

Trial Details

FieldValue
Enrollment Target 140 participants
Start Date 2026-07
Est. Completion 2029-07
Phase Phase 1
Clasp Therapeutics

2 total trials

What is known before NCT07650357 opens enrollment

NCT07650357 is an interventional study that assigns participants to a tested intervention. The registered 140 participants enrollment target is mid-sized for trials with a published cap, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (133% higher).

The record links to 0 conditions, and to 1 intervention - of which CLSP-5282 is the first listed.

NCT07650357 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT07650357 about?

NCT07650357 is a clinical study titled "A Study of CLSP 5282 in HLA-A*03:01 Positive Adult Patients With Solid Tumors (SENTINEL-101)". Phase 1, open-label, multicenter study to evaluate the safety, tolerability, PK, PD, and preliminary clinical activity of CLSP 5282 when administered to HLA A\*03:01-positive adult patients with advanced solid tumors that harbor the KRas G12V mutation.

What is the current status of trial NCT07650357?

This trial is currently not yet recruiting. It is a Phase 1 study. The enrollment target is 140 participants. The study started on 2026-07. Estimated completion is 2029-07.

What interventions are being tested in trial NCT07650357?

The interventions under investigation include: CLSP-5282 (DRUG).

Who is sponsoring clinical trial NCT07650357?

This trial is sponsored by Clasp Therapeutics, which has 2 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT07650357's enrollment target sits among peer trials

140 402nd of 2000 higher than 1,583 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT07650357, the US trial registry maintained by the National Library of Medicine. NCT07650357 (mid enrollment · none site footprint · not yet recruiting) retrieved and formatted by PlainTrial, see methodology.