Skip to content
Study details
Enrolling now

A Phase 1/2 Study of STP938 for Adult Subjects With Relapsed/Refractory B-Cell and T-Cell Lymphomas

Step Pharma, SAS
NCT IDNCT05463263ClinicalTrials.gov data as of Apr 2026
Phase

Phase 1/2

Target enrollment

180

Study length

about 3.4 years

Ages

18+

Locations

3 sites in CO, FL, NY

About this study

Researchers are testing a treatment called STP938 in adults with relapsed or refractory B-cell and T-cell lymphomas. The trial will first determine the best dose of STP938 to use, then expand it to include more patients who are receiving this treatment.

Based on ClinicalTrials.gov records.

What participants do

  • 1.Take STP938
PhasePhase 1/Phase 2
Primary goalObjective Response Rate (ORR) (Phase 2 / Dose Expansion)

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low15%
Logistics
Moderate50%

Logistics difficulty varies by site location and availability.

Trial highlights

Treatment details

Auto-extracted from trial records to preview treatments and outcomes.

Endpoints

Primary: Objective Response Rate (ORR) (Phase 2 / Dose Expansion), Safety and Tolerability (Phase 1 / Dose Escalation)

Secondary: Area under the curve (AUC) of STP938 including effects of food on absorption (Phase 1 / Dose Escalation), Evaluate best overall response of STP938 (Phase 1 / Phase 2), Evaluation Duration of Response (Phase 1 / Phase 2), Evaluation Progression Free Survival (Phase 1 / Phase 2), Evaluation of Complete Response Rate (Phase 2), Maximum plasma concentration (Cmax) of STP938 including effects of food on absorption (Phase 1 / Dose Escalation), Safety and Tolerability (Phase 2 / Dose Expansion), Time to reach maximum concentration (TMax) of STP938 including effects of food on absorption (Phase 1 / Dose Escalation)

Body systems

Oncology