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Spots Global Cancer Trial Database for Study of TBio-6517 Given Alone or in Combination With Pembrolizumab in Solid Tumors

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Trial Identification

Brief Title: Study of TBio-6517 Given Alone or in Combination With Pembrolizumab in Solid Tumors

Official Title: A Phase 1/2a, Multicenter, Open-label Trial of TBio-6517, an Oncolytic Vaccinia Virus, Administered Alone and in Combination With Pembrolizumab, in Patients With Advanced Solid Tumors

Study ID: NCT04301011

Study Description

Brief Summary: To determine the recommended Phase 2 dose (RP2D) of TBio-6517 when administered by direct injection into tumor(s) or intravenously and when combined with pembrolizumab in patients with solid tumors (RIVAL-01).

Detailed Description: This is a Phase 1/2a dose escalation study with TBio-6517 administered by direct injection into tumor(s) or by intravenous infusion. The Phase 1 portion has 4 arms; the first arm (Arm A) will determine the RP2D of TBio-6517 alone when directly injected into tumor(s), and the second arm (Arm B) will determine the RP2D of TBio-6517 when combined with pembrolizumab. The third and fourth arms will determine the RP2D of TBio-6517 when given intravenously alone and with pembrolizumab, respectively. In the Phase 2a portion, the clinical benefit of TBio-6517 combined with pembrolizumab will be further explored in patients with Microsatellite Stable Colorectal Cancer (MSS-CRC), Cholangiocarcinoma (CCA), Cutaneous Melanoma, and Cutaneous Squamous Cell Carcinoma of the Skin (cSCC), as assessed by overall response rate (ORR) from central radiology review.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Mayo Clinic, Phoenix, Arizona, United States

Mayo Clinic, Jacksonville, Florida, United States

Sylvester Comprehensive Cancer Center / UMHC, Miami, Florida, United States

University of Kansas Medical Center, Kansas City, Kansas, United States

Clinical Site 1007, Boston, Massachusetts, United States

Mayo Clinic, Rochester, Minnesota, United States

The Billings Clinic, Billings, Montana, United States

University of Texas MD Anderson Cancer Center, Houston, Texas, United States

Ottawa Hospital and Research Institute (OHRI), Ottawa, Ontario, Canada

National Cancer Center, Ilsandong, , Korea, Republic of

Seoul National University Hospital (SNUH), Junggu, , Korea, Republic of

Contact Details

Name: Ines Verdon, MD

Affiliation: Turnstone Biologics

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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