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Safety, Pharmacokinetics (PK), and Efficacy of ONC 841 in Advanced Solid Tumors - Trial NCT06352359

Access comprehensive clinical trial information for NCT06352359 through Pure Global AI's free database. This Phase 1 trial is sponsored by OncoC4, Inc. and is currently Not yet recruiting. The study focuses on Advanced Solid Tumor. Target enrollment is 30 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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NCT06352359
Phase 1
Not yet recruiting
drug
Trial Details
ClinicalTrials.gov โ€ข NCT06352359
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Safety, Pharmacokinetics (PK), and Efficacy of ONC 841 in Advanced Solid Tumors

Study Focus

Advanced Solid Tumor

ONC-841

Interventional

drug

Sponsor & Location

OncoC4, Inc.

Sacramento,Louisville,Houston, United States of America

Timeline & Enrollment

Phase 1

Jun 30, 2024

Jun 30, 2027

30 participants

Primary Outcome

Dose Limiting Toxicity (DLT),Maximum Toxicity Dose (MTD)

Summary

This is a Phase I open label, dose-escalation study of intravenous (IV) infusion of ONC-841
 as a single agent in patients with advanced/metastatic solid tumors. The study will evaluate
 seven dose levels of ONC-841 starting from 0.03 mg/kg to 30 mg/kg.

ICD-10 Classifications

Carcinoma in situ, unspecified
Malignant neoplasm: Prepuce
Malignant neoplasm: Connective and soft tissue, unspecified
Malignant neoplasm: Parametrium
Malignant neoplasm of other connective and soft tissue

Data Source

ClinicalTrials.gov

NCT06352359

Non-Device Trial