Soquelitinib vs Standard of Care in Participants With Relapsed/Refractory Peripheral T-cell Lymphoma Not Otherwise Specified, Follicular Helper T-cell Lymphomas, or Systemic Anaplastic Large-cell Lymphoma

Phase 3

Recruiting

• Conditions: Systemic Anaplastic Large Cell Lymphoma; Peripheral T-Cell Lymphoma, Not Otherwise Specified; Angioimmunoblastic T-cell Lymphoma; Lymphoma, T-Cell, Peripheral; Follicular T-Cell Lymphoma; Nodal Peripheral T-Cell Lymphoma With TFH Phenotype; Lymphoma, T-Cell
• Interventions: Drug: Soquelitinib; Drug: Belinostat; Drug: Pralatrexate

• Registration Number: NCT06561048
• Lead Sponsor: Corvus Pharmaceuticals, Inc.

Brief Summary

A Phase 3, randomized, 2-arm, open-label, multicenter, stratified study of soquelitinib versus physician's choice standard of care (SOC) treatment (selected single agents) in participants with relapsed/refractory (R/R) peripheral T-cell lymphoma not otherwise specified (PTCL-NOS), follicular helper T-cell lymphomas (FHTCLs), or systemic anaplastic large-cell...

Detailed Description

This is a Phase 3, randomized, 2-arm, open-label, multicenter, stratified study of soquelitinib, an oral interleukin-2-inducible T cell kinase (ITK) inhibitor, versus physician's choice standard of care (SOC) treatment of either belinostat or pralatrexate in participants with relapsed/refractory (R/R) peripheral T-cell lymphoma not otherwise specified (PTCL-...

Basic Information
|
Recruitment & Eligibility
|
Study & Design
|
Trial Locations
|
Related News

Study Timeline

• Study First Submitted: 2024-08-16
• Study First Submitted QC: 2024-08-16
• Study First Posted: 2024-08-19
• Status Verified: 2024-10
• Study Start: 2024-10-02
• Last Update Submitted: 2024-10-17
• Last Update Posted: 2024-10-21
• Primary Completion: 2026-02
• Study Completion: 2027-09

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 150

Inclusion Criteria

1. Adult participants ≥18 years of age on the day of signing the informed consent form.

2. Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 to 2.

3. Histologically confirmed PTCL-NOS, FHTCLs or sALCL per The International Consensus Classification of Mature Lymphoid Neoplasms.

4. Progressed on, be refractory to, relapsed, or intolerant to standard therapy for their cancer. At least 1 but not more than 3 prior systemic therapies.

5. Fluorodeoxyglucose-avid disease by positron emission tomography and measurable disease of at least 1.5 cm by computed tomography, as assessed by the site radiologist.

6. Life expectancy >12 weeks.

7. Adequate organ function as determined by:

   • Absolute neutrophil count ≥ 1.0×10^9/L (1000/mm3) (without receiving granulocyte-colony stimulating factor)
   • Platelet count ≥ 50×10^9/L (without transfusion)
   • Hemoglobin ≥ 9.0 g/dL, without packed red blood cell transfusion within the last 1 week of starting study drug
   • Prothrombin time international normalized ratio and partial thromboplastin time ≤1.5 × upper limit of normal (ULN), unless participant is receiving anticoagulant therapy and prothrombin time or activated partial thromboplastin time is within therapeutic range of intended use of anticoagulants
   • Calculated creatinine clearance (CrCl) according to Cockcroft-Gault formula and based on ideal body weight or 24-hour urine CrCl ≥ 50 mL/minute
   • Total bilirubin ≤ 1.5 × ULN or direct bilirubin ≤ ULN for participants with total bilirubin levels > 1.5 × ULN. For participants with Gilbert's disease: ≤ 3.0 mg/dL or discussion with the Medical Monitor
   • Aspartate aminotransferase and alanine transaminase ≤ 2.5 × ULN (≤ 5 × ULN for participants with liver metastases)
   • Serum albumin > 2.5 g/dL
   • Serum calcium < 12 mg/dL or corrected serum calcium < ULN

8. Female participants of childbearing potential who are sexually active with a non-sterilized male partner must agree to use at least 1 highly effective method of contraception from the time of screening and must agree to continue using such precautions for 120 days after the last dose of study drug for participants who receive soquelitinib, or 6 months after the last dose for participants who receive either belinostat or pralatrexate.

9. Non-sterilized males who are sexually active with a female partner of childbearing potential must use a condom plus spermicide from Day 1 through 120 days after the last dose of study drug.

Read More

Exclusion Criteria

1. Participants who have T-cell lymphoma with active central nervous system involvement.
2. Any significant medical condition, laboratory abnormality, or psychiatric illness that would prevent the participant from participating in the study.
3. Any condition that confounds the ability to interpret data from the study.
4. Any active infection requiring IV therapy.
5. History of invasive prior malignancy that required systemic therapy within last 3 years.
6. Known to be positive for HIV, or positive test for chronic hepatitis B virus (HBV) infection (defined as positive hepatitis B surface antigen [HBsAg]) or positive test for hepatitis C antibody.
7. Monoclonal antibody therapy for cancer, radiotherapy, or chemotherapy within 3 weeks and targeted therapy within 2 weeks prior to the first dose of study treatment.
8. History of allogeneic hematopoietic stem cell transplantation.
9. Candidate for hematopoietic stem cell transplantation at screening.
10. History of progressive disease within 6 months of autologous hematopoietic stem cell transplantation.
11. Females who are pregnant, lactating, or intend to become pregnant during their participation in the study, starting with the screening visit through 6 months after the last dose of study treatment.

Read More

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Soquelitinib	Soquelitinib	Participants will administer soquelitinib 200 mg orally twice daily for up to 2 years
Standard of Care	Belinostat	Participants will receive physician's choice standard of care treatment of either pralatrexate or belinostat for up to 2 years
Standard of Care	Pralatrexate	Participants will receive physician's choice standard of care treatment of either pralatrexate or belinostat for up to 2 years

Primary Outcome Measures

Name	Time	Method
Progression-free survival	Up to 4 years post study treatment initiation	Time from first study treatment to first occurrence of progression (as assessed by the Independent Review Committee) or death, whichever occurs first

Secondary Outcome Measures

Name	Time	Method
Overall survival	Up to 4 years post study treatment initiation	Time from first study treatment to death from any cause
Objective response rate	Up to 2 years post study treatment initiation	The rate of participants who achieve a partial response or complete response as assessed by the Independent Review Committee according to the Revised Criteria for Response Assessment of Malignant Lymphoma (Lugano Classification 2014), and modified Severity Weighted Assessment Tool (mSWAT) for participants with skin involvement

Trial Locations

Locations (1)

Corvus Clinical Trials Information; 🇺🇸 Burlingame, California, United States