NCT06307925

A Phase I Study to Evaluate the Safety, Pharmacokinetics and Antitumor Activity of HC010 in Patients With Advanced Solid Tumors

A Phase I Open-label, Multi-center, Dose Escalation and Expansion Study to Evaluate the Safety, Pharmacokinetics and Antitumor Activity of HC010 in Patients With Advanced Solid Tumors
HC Biopharma Inc.·Phase 1·ClinicalTrials.gov·drugRecruiting
View on ClinicalTrials.gov
Study focus
Disease/Condition
Advanced Solid Tumor
Drug/Device/Intervention
HC010
Study type
Interventional
Intervention type
drug
Sponsor & location
Primary sponsor
HC Biopharma Inc.
Location
Guangzhou, China
Timeline & enrollment
Phase
Phase 1
Start date
Mar 27, 2024
End date
Dec 31, 2025
Enrollment
122 participants
Primary outcome

Incidence of dose-limiting toxicity,Adverse events,serious adverse events,Maximum Tolerated Dose,Recommended Dose for Phase II Clinical Studies

Summary

This clinical trial is a multicenter, open, single-arm, non-randomized, dose-escalation and
 dose-expansion, phase I clinical study in patients with advanced recurrent or metastatic
 solid tumors.The goal of this study is to evaluate the safety and tolerability of HC010
 monotherapy in patients with advanced solid tumors.

ICD-10 classifications
Carcinoma in situ, unspecifiedMalignant neoplasm: PrepuceMalignant neoplasm: Connective and soft tissue, unspecifiedMalignant neoplasm: ParametriumMalignant neoplasm of other connective and soft tissue
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT06307925
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT06307925 through Pure Global AI's free database. This Phase 1 trial is sponsored by HC Biopharma Inc. and is currently Recruiting. The study focuses on Advanced Solid Tumor. Target enrollment is 122 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.