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CAN1012 Combined With PD-1 in Patients With Solid Tumors - Trial NCT06410703

Access comprehensive clinical trial information for NCT06410703 through Pure Global AI's free database. This Phase 1/2 trial is sponsored by Canwell Biotech Limited and is currently Not yet recruiting. The study focuses on Advanced Solid Tumor. Target enrollment is 71 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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NCT06410703
Phase 1/2
Not yet recruiting
drug
Trial Details
ClinicalTrials.gov โ€ข NCT06410703
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CAN1012 Combined With PD-1 in Patients With Solid Tumors
A Phase Ib/IIa, Dose Escalation, Open-Label Study of Intratumoral CAN1012 Combined With PD-1 in Patients With Unresectable or Metastatic Advanced Solid Tumors

Study Focus

Advanced Solid Tumor

CAN1012

Interventional

drug

Sponsor & Location

Canwell Biotech Limited

Guangzhou, China

Timeline & Enrollment

Phase 1/2

May 30, 2024

May 30, 2026

71 participants

Primary Outcome

Safety and tolerability

Summary

This is a Phase Ia/IIb, open-label, first-in-human, multicenter, single-arm, dose escalation
 study of intratumoral CAN1012 combined with PD-1 in patients with Unresectable or Metastatic
 Advanced Solid Tumors who have exhausted options for standard of care therapy.

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

NCT06410703

Non-Device Trial