Last reviewed · How we verify

NCT05431582

Phase I Study of ZN-c3 and Bevacizumab ± Pembrolizumab in Metastatic CCNE1 Amplified and TP53 Mutant Solid Tumors

Withdrawn Phase 1 Last updated 15 June 2023
What this trial tests

Phase 1 trial testing ZN-c3 in Tumors. Withdrawn.

Timeline
14 December 2022
Primary endpoint
14 December 2022
14 December 2022

Quick facts

Lead sponsorM.D. Anderson Cancer Center
PhasePhase 1
StatusWithdrawn
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Start date14 December 2022
Primary completion14 December 2022
Estimated completion14 December 2022

Drugs / interventions tested

Conditions studied

Sponsor

M.D. Anderson Cancer Center — full company profile →

Who can join

18 and older, any sex, with Tumors or Ovarian Cancer. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Primary Objectives are to determine the maximum tolerated dose (MTD)/recommended phase 2 dose (RP2D) of ZN-c3 and ZN-c3 and bevacizumab or ZN-c3 and bevacizumab plus pembrolizumab in metastatic CCNE1 amplified and TP53 mutant solid tumors as well to evaluate antitumor activity of ZN-c3 and bevacizumab or ZN-c3 and bevacizumab plus pembrolizumab in metastatic CCNE1 amplified and TP53 mutant solid tumors.

Publications & conference data

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

  1. Targeting the DNA damage response for cancer therapy.
    Curtin NJ. · · 2023 · cited 30× · PMID 36606678 · DOI 10.1042/bst20220681
  2. Combination, Modulation and Interplay of Modern Radiotherapy with the Tumor Microenvironment and Targeted Therapies in Pancreatic Cancer: Which Candidates to Boost Radiotherapy?
    Benkhaled S, Peters C, Jullian N, Arsenijevic T, et al · · 2023 · cited 19× · PMID 36765726 · DOI 10.3390/cancers15030768
  3. Synthetic and Medicinal Chemistry Approaches Toward WEE1 Kinase Inhibitors and Its Degraders.
    Alli VJ, Yadav P, Suresh V, Jadav SS. · · 2023 · cited 18× · PMID 37323408 · DOI 10.1021/acsomega.3c01558
  4. Advancing cancer therapy: new frontiers in targeting DNA damage response.
    Qian J, Liao G, Chen M, Peng RW, et al · · 2024 · cited 16× · PMID 39372203 · DOI 10.3389/fphar.2024.1474337
  5. The Combination of Immune Checkpoint Blockade with Tumor Vessel Normalization as a Promising Therapeutic Strategy for Breast Cancer: An Overview of Preclinical and Clinical Studies.
    Melaiu O, Vanni G, Portarena I, Pistolese CA, et al · · 2023 · cited 14× · PMID 36834641 · DOI 10.3390/ijms24043226
  6. Targeting the DNA damage response in cancer.
    Federica G, Michela C, Giovanna D. · · 2024 · cited 12× · PMID 39492835 · DOI 10.1002/mco2.788
  7. Exploiting DNA Replication Stress as a Therapeutic Strategy for Breast Cancer.
    Zhang J, Chan DW, Lin SY. · · 2022 · cited 12× · PMID 36359297 · DOI 10.3390/biomedicines10112775
  8. Targeting WEE1 Kinase in Gynecological Malignancies.
    Zhang W, Li Q, Yin R. · · 2024 · cited 8× · PMID 38915863 · DOI 10.2147/dddt.s462056

Verify or expand the search:

Other trials of ZN-c3

Trials testing the same drug.

Other recruiting trials for Tumors

Currently open trials in the same condition.

Other M.D. Anderson Cancer Center trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05431582.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing