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NCT06417554

A Phase IB /II, Multicenter, Open-Label Study of Safety, Tolerability and Efficacy of SHR-A2102 for Injection With or Without Antitumor Therapy in Subjects With Advanced Solid Tumors

Recruiting now Phase 1/Phase 2 Last updated 29 December 2024
What this trial tests

Phase 1/Phase 2 trial testing SHR-A2102 in Advanced Solid Tumors in 80 participants. Currently enrolling.

Timeline
13 May 2024
Primary endpoint
1 July 2027
1 July 2027

Quick facts

Lead sponsorShanghai Hengrui Pharmaceutical Co., Ltd.
PhasePhase 1/Phase 2
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment80
Start date13 May 2024
Primary completion1 July 2027
Estimated completion1 July 2027
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Shanghai Hengrui Pharmaceutical Co., Ltd. — full company profile →

Who can join

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

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

The study is being conducted to evaluate the safety, tolerability and efficacy of SHR-A2102 for injection with or without Antitumor Therapy in Advanced Solid Tumors. To explore the reasonable dosage of SHR-A2102 for Advanced Solid Tumors.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of SHR-A2102

Trials testing the same drug.

Other recruiting trials for Advanced Solid Tumors

Currently open trials in the same condition.

Other Shanghai Hengrui Pharmaceutical Co., Ltd. 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/NCT06417554.

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