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Spots Global Cancer Trial Database for A Study of Mipasetamab Uzoptirine (ADCT-601) in Participants With Solid Tumors

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Trial Identification

Brief Title: A Study of Mipasetamab Uzoptirine (ADCT-601) in Participants With Solid Tumors

Official Title: A Phase 1b, Open-Label, Dose-Escalation and Dose-Expansion Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Antitumor Activity of Mipasetamab Uzoptirine (ADCT-601) Monotherapy and in Combination With Other Anti-Cancer Therapies in Patients With Selected Advanced Solid Tumors

Study ID: NCT05389462

Interventions

ADCT-601
Gemcitabine

Study Description

Brief Summary: The primary objective of this study is to identify the recommended phase 2 dose (RP2D) and/or the maximum tolerated dose (MTD), and characterize the safety and tolerability of ADCT-601 monotherapy and in combination with gemcitabine.

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Sarcoma Oncology Research Center, Santa Monica, California, United States

Stanford Cancer Center, Stanford Medicine at Stanford University, Stanford, California, United States

University of IOWA, Iowa City, Iowa, United States

Washington University School of Medicine, Saint Louis, Missouri, United States

Sarah Cannon at University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma, United States

Vanderbilt University Medical Center (VUMC) - Ingram Cancer Center, Nashville, Tennessee, United States

Institut Bergonié, Bordeaux, Gironde, France

Institut Léon Bérard, Lyon, , France

Centre Antoine Lacassagne, Nice, , France

Hospital Universitario Vall d'Hebron, Barcelona, , Spain

Hospital Universitario Fundacion Jimenez Diaz, Madrid, , Spain

Hospital Universitario Madrid Sanchinarro, Madrid, , Spain

The Christie NHS Foundation Trust, Manchester, , United Kingdom

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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