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Phase 1 Trial of KH801 - Trial NCT06364501

Access comprehensive clinical trial information for NCT06364501 through Pure Global AI's free database. This Phase 1 trial is sponsored by Beijing Kanghong Biopharmaceutical Co., Ltd. and is currently Not yet recruiting. The study focuses on Advanced Solid Tumors. Target enrollment is 17 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.

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NCT06364501
Phase 1
Not yet recruiting
drug
Trial Details
ClinicalTrials.gov โ€ข NCT06364501
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Phase 1 Trial of KH801
A Phase I Clinical Study Evaluating the Safety, Tolerability, Pharmacokinetic Characteristics, and Preliminary Anti-tumor Activity of KH801 Injection in Patients With Advanced Solid Tumors

Study Focus

Advanced Solid Tumors

KH801

Interventional

drug

Sponsor & Location

Beijing Kanghong Biopharmaceutical Co., Ltd.

Chengdu Kanghong Pharmaceutical Group Co., Ltd.

Peking,Guangzhou,Jinan,Chengdu, China

Timeline & Enrollment

Phase 1

May 01, 2024

May 01, 2030

17 participants

Primary Outcome

MTD,DLT,RP2D

Summary

KH801 is a injection used for advanced solid tumors which must be diluted with 5% Dextrose Or
 0.9% sodium chloride Injection.
 
 This study is expected to include a total of approximately 17-42 participants.

ICD-10 Classifications

Malignant neoplasm: Prepuce
Carcinoma in situ, unspecified
Malignant neoplasm: Connective and soft tissue, unspecified
Malignant neoplasm: Parametrium
Malignant neoplasm: Orbit

Data Source

ClinicalTrials.gov

NCT06364501

Non-Device Trial