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NCT03944902: BRCA

CB-839 in Combination With Niraparib in Platinum Resistant BRCA -Wild-type Ovarian Cancer Patients

Terminated Phase 1 Last updated 21 November 2023
What this trial tests

Phase 1 trial testing Cohort 1: Dose Escalation in Ovarian Cancer in 1 participant. Terminated before completion.

Timeline
1 September 2021
Primary endpoint
5 January 2022
5 January 2022

Quick facts

Lead sponsorUniversity of Alabama at Birmingham
PhasePhase 1
StatusTerminated
Study typeINTERVENTIONAL
Allocationnon randomized
Designsequential
Maskingnone
Primary purposetreatment
Enrollment1
Start date1 September 2021
Primary completion5 January 2022
Estimated completion5 January 2022
Sites4 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

University of Alabama at Birmingham

Who can join

18 and older, female only, with Ovarian Cancer or Resistant BRCA Wild-Type Ovarian Cancer. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this protocol is to investigate the efficacy of the combination of CB-839 with Niraparib in platinum resistant BRCA wild-type ovarian cancer patients. The primary and secondary objectives are to determine the maximum tolerated dose of CB-839 in combination with Niraparib and to determine the response rate and percentage of participants who remain progression free at 6 months.

Publications & conference data

8 peer-reviewed publications reference this trial (live from Europe PMC):

  1. Enhancing the Efficacy of Glutamine Metabolism Inhibitors in Cancer Therapy.
    Yang WH, Qiu Y, Stamatatos O, Janowitz T, et al · · 2021 · cited 222× · PMID 34020912 · DOI 10.1016/j.trecan.2021.04.003
  2. Mitochondrial adaptation in cancer drug resistance: prevalence, mechanisms, and management.
    Jin P, Jiang J, Zhou L, Huang Z, et al · · 2022 · cited 180× · PMID 35851420 · DOI 10.1186/s13045-022-01313-4
  3. A glutamine tug-of-war between cancer and immune cells: recent advances in unraveling the ongoing battle.
    Wang B, Pei J, Xu S, Liu J, et al · · 2024 · cited 81× · PMID 38459595 · DOI 10.1186/s13046-024-02994-0
  4. Metabolic Regulation of Redox Balance in Cancer.
    Purohit V, Simeone DM, Lyssiotis CA. · · 2019 · cited 79× · PMID 31288436 · DOI 10.3390/cancers11070955
  5. Inhibition of glutaminolysis in combination with other therapies to improve cancer treatment.
    Shen YA, Chen CL, Huang YH, Evans EE, et al · · 2021 · cited 61× · PMID 33721588 · DOI 10.1016/j.cbpa.2021.01.006
  6. Role of glutamine and its metabolite ammonia in crosstalk of cancer-associated fibroblasts and cancer cells.
    Li X, Zhu H, Sun W, Yang X, et al · · 2021 · cited 48× · PMID 34503536 · DOI 10.1186/s12935-021-02121-5
  7. Thiadiazole derivatives as anticancer agents.
    Szeliga M. · · 2020 · cited 41× · PMID 32880874 · DOI 10.1007/s43440-020-00154-7
  8. Rethinking glutamine metabolism and the regulation of glutamine addiction by oncogenes in cancer.
    Ni R, Li Z, Li L, Peng D, et al · · 2023 · cited 38× · PMID 36959802 · DOI 10.3389/fonc.2023.1143798

Verify or expand the search:

Other recruiting trials for Ovarian Cancer

Currently open trials in the same condition.

Other University of Alabama at Birmingham trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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