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NCT06763159

A Study of HS-20124 in Patients with Advanced Solid Tumors

Recruiting now Phase 1 Last updated 8 January 2025
What this trial tests

Phase 1 trial testing HS-20124 (Phase Ia:Dose escalation ) in Solid Cancer in 450 participants. Currently enrolling.

Timeline
30 October 2024
Primary endpoint
31 December 2026
31 December 2027

Quick facts

Lead sponsorHansoh BioMedical R&D Company
PhasePhase 1
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationnon randomized
Designsequential
Maskingnone
Primary purposetreatment
Enrollment450
Start date30 October 2024
Primary completion31 December 2026
Estimated completion31 December 2027
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Hansoh BioMedical R&D Company — full company profile →

Who can join

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

Sponsor's own description

HS-20124 is a novel DAR-8 antibody-drug conjugate (ADC) targeting CDH6. In preclinical studies, it inhibited tumor cell growth expressing CDH6 in vitro and in vivo. The first-in-human trial is conducted to assess the maximum tolerated dose (MTD) and dose limiting toxicity (DLT), to evaluate the pharmacokinetics, safety and preliminary anti-tumor activity of HS-20124 in Patients With Advanced Solid Tumors.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Solid Cancer

Currently open trials in the same condition.

Other Hansoh BioMedical R&D Company 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/NCT06763159.

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