Last reviewed · How we verify

NCT06992687

A Study to Evaluate the Safety and Efficacy of HB0052 in Patients With Advanced Solid Tumors

ENROLLING BY INVITATION Phase 1, PHASE2 Last updated 28 May 2025
What this trial tests

Phase 1, PHASE2 trial testing HB0052 Injection in Solid Tumors in 30 participants. Enrolling by invitation.

Timeline
1 September 2024
Primary endpoint
30 September 2025
30 November 2025

Quick facts

Lead sponsorShanghai Huaota Biopharmaceutical Co., Ltd.
PhasePhase 1, PHASE2
StatusENROLLING BY INVITATION
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment30
Start date1 September 2024
Primary completion30 September 2025
Estimated completion30 November 2025
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Shanghai Huaota Biopharmaceutical Co., Ltd. — full company profile →

Who can join

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

Sponsor's own description

To evaluate the safety and tolerability of HB0052 in patients with advanced solid tumors

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

Verify or expand the search:

Other recruiting trials for Solid Tumors

Currently open trials in the same condition.

Other Shanghai Huaota Biopharmaceutical 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/NCT06992687.

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