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Spots Global Cancer Trial Database for Phase 1/2 Study of OBI-999 in Patients With Advanced Solid Tumors

The following info and data is provided "as is" to help patients around the globe.
We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Phase 1/2 Study of OBI-999 in Patients With Advanced Solid Tumors

Official Title: A Phase 1/2, Open-Label, Dose-Escalation and Cohort-Expansion Study Evaluating the Safety, Pharmacokinetics, and Therapeutic Activity of OBI-999 in Patients With Advanced Solid Tumors

Study ID: NCT04084366

Interventions

OBI-999
OBI-999

Study Description

Brief Summary: The purpose of this study is to establish the maximum tolerated dose (MTD) and recommended phase 2 dose (RP2D) of OBI-999 as monotherapy, and to characterize the safety and preliminary clinical activity profile of the RP2D of OBI-999 in patients with advanced solid tumors.

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Scripps MD Anderson Cancer Center, La Jolla, California, United States

Memorial Sloan Kettering Cancer Center, New York, New York, United States

West Cancer Center, Germantown, Tennessee, United States

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

Contact Details

Name: Apostolia Tsimberidou, MD, PhD

Affiliation: M.D. Anderson Cancer Center

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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