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NCT07461181

A Study to Evaluate the Safety, Tolerability, PK, PD, and Preliminary Efficacy of CS01 in Patients With Locally Advanced or Metastatic Solid Tumors

Active, enrolled Phase 1, PHASE2 Last updated 10 March 2026
What this trial tests

Phase 1, PHASE2 trial testing CS01 (an anti-OX40 antibody) in Locally Advanced or Metastatic Solid Tumors in 10 participants. Participants enrolled and being followed up; not accepting new ones.

Timeline
30 December 2024
Primary endpoint
31 December 2026
31 December 2026

Quick facts

Lead sponsorRuijin Hospital
PhasePhase 1, PHASE2
StatusActive, enrolled
Study typeINTERVENTIONAL
Allocationnon randomized
Designsequential
Maskingnone
Primary purposetreatment
Enrollment10
Start date30 December 2024
Primary completion31 December 2026
Estimated completion31 December 2026
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Ruijin Hospital

Who can join

18 and older, any sex, with Locally Advanced or Metastatic Solid Tumors. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is an investigator-initiated clinical trial evaluating the safety, tolerability, pharmacokinetics, pharmacodynamics, and preliminary efficacy of CS01 in patients with locally advanced or metastatic solid tumors.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Locally Advanced or Metastatic Solid Tumors

Currently open trials in the same condition.

Other Ruijin Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07461181.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing