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Study details
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A Study of CS5001 in Patients With Advanced Solid Tumors and Lymphomas

CStone Pharmaceuticals
NCT IDNCT05279300ClinicalTrials.gov data as of Apr 2026
Phase

Phase 1

Target enrollment

480

Study length

about 5.8 years

Ages

18+

Locations

3 sites in NY, TX

What this study is about

This trial is testing the safety and preliminary effectiveness of a new drug called CS5001 in people with advanced lymphoma or solid tumors. The treatment will be given as a single agent or in combination with other medications.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Receive Rituximab
  • 2.Take CS5001
  • 3.Take Cyclophosphamide
  • +3 more

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Injection / IVInjection / IV

How treatment is administered

Treatment Assignment
All receive treatment

Everyone gets the investigational treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Drug classes

cyclophosphamide (Alkylating chemotherapy; crosslinks DNA strands), doxorubicin (Anthracycline chemotherapy; intercalates DNA and inhibits topoisomerase II), gemcitabine, lenalidomide (Immunomodulatory drug; affects immune system and cancer cells (exact mechanism unclear)), oxaliplatin, prednisone, rituximab (Monoclonal antibody; targets CD20 on B-cells to destroy them), vincristine

Drug routes

infusion, injection (Injection), oral (Oral Capsule), oral

Endpoints

Primary: Incident and severity of adverse events, Maximum Tolerated Dose (MTD) of CS5001 if any (for dose escalation part), Objective Response Rate (ORR) (for dose expansion)

Body systems

Oncology