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Clinical Trial ● Currently Recruiting Phase I NCT06297525

Study of STP938 in Advanced Solid Tumours

Study of STP938 in Advanced Solid Tumours — Recruiting • Phase I • Oncology • NCT06297525.

📅 23 Apr 2026 ⏱ 2 min read
Currently Recruiting
This trial is actively seeking participants in the UK. Discuss eligibility with your patient before referring.
Status
Currently Recruiting
Phase
Phase I
NCT ID
NCT06297525
Sponsor
Step Pharma, SAS
Start
2024-08-02
ClinicaliQ Trial Snapshot
  • Study of STP938 in Advanced Solid Tumours — Recruiting • Phase I • Oncology • NCT06297525.
  • What is being tested: STP938 is an investigational drug being evaluated in a Phase 1 dose escalation and safety expansion study as a monotherapy treatment in patients with advanced solid tumours, with the aim of determining optimal dosing and safety profile.
  • Patient eligibility overview: The trial recruits patients with advanced solid tumours who are typically treatment-experienced or unsuitable for standard therapies; specific inclusion/exclusion criteria are determined by the trial protocol and assessed at individual trial sites.
Use This Page For
  • Quick orientation before opening the registry record.
  • Checking recruitment status, phase and sponsor at a glance.
  • Connecting this trial to nearby guidelines, Drug Science and education.
What This Trial Is Studying

The Phase 1a part of the study is a dose escalation of STP938 as a monotherapy. The Phase 1b part of the study is a safety expansion cohort of STP938 as a monotherapy.

Eligibility Snapshot
  • Main Inclusion Criteria: * Signed and dated informed consent, and able to comply with the study procedures and any locally required authorization. * Male or female aged ≥ 18 years. * Advanced disease not curable by available therapies and requires systemic therapy. * Histologically confirmed diagnosis of eligible cancer type. * Must have tumor tissue available for biomarker testing. * Measurable disease (Part 1) and measurable disease per RECIST (Part2) * Eastern Cooperative Oncology Group (ECOG) performance status ≤2. * Life expectancy > 3 months as assessed by the Investigator. * Adequate organ function (bone marrow, hepatic, renal function and coagulation). * All toxicities (except alopecia) from prior cancer treatments or procedures must have resolved to ≤Grade 1 or returned to baseline levels prior to enrollment. Main

Use the source registry for the full inclusion and exclusion criteria before discussing referral or enrolment.

Full Trial Details
View this trial on the source registry
Eligibility criteria, protocol, and results when available
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