Clinical Trials

Sara's Cure

To Evaluate Maximally Tolerated Dose (MTD), Safety and Efficacy of CPI-613® (Devimistat) Plus Hydroxychloroquine in Patients With Relapsed or Refractory Clear Cell Sarcoma of Soft Tissue

Sponsor: 

Rafael Pharmaceuticals Inc.

Description: 

PHASE I / PHASE II:

The goal of this trial in Phase I is to determine the maximally tolerated dose (MTD) of hydroxychloroquine in combination with devimistat in patients with relapsed or refractory Clear Cell Sarcomas of the Soft Tissue and to describe the full toxicity profile. In Phase II, the goal is to evaluate the response rate [Complete Rate (CR) + Partial Rate (PR)] of the combination of devimistat and hydroxychloroquine in patients with relapse or refractory Clear Cell Sarcoma of the Soft Tissue and to evaluate the PK and PK/PD profiles for efficacy and safety of the combination of devimistat and hydroxychloroquine.

Clinical Trials Gov #: 

NCT04593758

Contact: 

sanjeev.luther@rafaelpharma.com

Supporting Publications: 

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5991736/ 

Testing Atezolizumab in patients >= 2 years old with Newly Diagnosed, Unresectable, or Metastatic Clear Cell Sarcoma or Chondrosarcoma

Sponsor:

National Cancer Institute (NCI)

Description:

This phase II trial studies how well atezolizumab works in treating patients with chondrosarcoma or clear cell sarcoma that is newly diagnosed, cannot be removed by surgery (unresectable), or has spread to other places in the body (metastatic). Immunotherapy with monoclonal antibodies, such as atezolizumab, may help the body’s immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread.

Clinical Trials Gov #: 

NCT04458922

Contact: 

National Cancer Institute Developmental Therapeutics Clinic
Bethesda, Maryland, United States, 2089
Contact: 800-411-1222
Principal Investigator: A P. Chen

Supporting Publications: 

CTOS 2018 

QUILT-3.031: AMG 337 in Subjects With Advanced or Metastatic Clear Cell Sarcoma

Sponsor:

NantPharma, LLC

Description:

The phase 2 single arm study will assess efficacy of AMG 337 (based on confirmed ORR) in subjects with advanced or metastatic clear cell sarcoma that contains the EWSR1-ATF1 gene fusion, as determined by fluorescent in situ hybridization (FISH) or other diagnostic methods and confirmed by RNA sequencing (RNAseq).

Clinical Trials Gov #: 

NCT03132155 

Contact: 

Liza H Ochoa, BS 

310-912-2475 QUILT3031@NantPharma.com 

Supporting Publications: 

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