Sun Yat-Sen University Sun Yat-Sen Memorial Hospital
Guangzhou, Guangdong, 510535, China
Location status: Recruiting
Location contact
Herui Yao, Professor
CONTACT
NCT Number: NCT06332430
A phase 1, dose escalation, open-label study of intratumoral CAN2109 in subjects with unstable or metastatic advanced solid tumors or lymphomas.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Phase 1
Guangzhou, Guangdong, 510535, China
Location status: Recruiting
Herui Yao, Professor
CONTACT
The scope of the study is to evaluate the safety of CAN2109 in humans, explore its safety, efficacy and collect data on the pharmacokinetics, as well as on the pharmacodynamic effect of the drug on the immune system locally and systemically, and on tumor markers.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
a. Carcinoma of skin, melanoma, Merkel cell carcinoma (MCC), breast cancer, head and neck squamous cell carcinoma (HNSCC), sarcoma, cervical carcinoma, and colorectal cancer
Exclusion criteria
CAN2109 IT injection (once every 3 weeks)
Time frame: 12 months
determined by assessment of dose limiting toxicities per protocol of CAN2109 with cancers.
Time frame: 12 months
To determine a recommended phase 2 dose of CAN21909 for further development by evaluating number of patients with treatment-related adverse events as assessed by the Common Terminology Criteria for Adverse Events version 5.0 (CTCAE v5.0).
Time frame: 12 months
determined by assessment of the maximum tolerated dose or maximal assessed dose per protocol of CAN2109 with cancers.
Time frame: 12 months
Proportion of patients experiencing a tumor response or a stable disease according to RECIST 1.1 or iRECIST 1.1 as appropriate.
Time frame: 12 months
Maximum observed plasma and tumor concentration of CAN2109 after IT administration.
Contact information is provided by the study sponsor or research team.
Erwei Song, MD
CONTACT
Herui Yao, MD
CONTACT
Canwell Biotech Limited
Industry
A Phase 1, Dose Escalation, Open-Label Study of Intratumoral CAN2109 in Subjects With Unresectable or Metastatic Advanced Solid Tumors.
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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