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ePoster Display

562TiP - A phase Ib dose-escalation study of ZN-c3, a WEE1 inhibitor, in combination with chemotherapy in patients with platinum-resistant or -refractory ovarian, peritoneal, or fallopian tube cancer

Date

16 Sep 2021

Session

ePoster Display

Topics

Clinical Research

Tumour Site

Ovarian Cancer

Presenters

Siqing Fu

Citation

Annals of Oncology (2021) 32 (suppl_5): S583-S620. 10.1016/annonc/annonc699

Authors

S. Fu1, A. Pasic2, G. Richardson3, Z.J. Vranjes4, T. Meniawy5, P.R. de Jong6, F. Donate6, A.A. Samatar6, J. Rodriguez7, P. Pultar7, D. Voliotis7

Author affiliations

  • 1 Investigational Cancer Therapeutics, University of Texas M.D. Anderson Cancer Center, 77030 - Houston/US
  • 2 Medical Oncology, Clinical Centre University of Sarajevo, 71000 - Sarajevo/BA
  • 3 Medical Oncology, Cabrini Hospital Malvern, Melbourne/AU
  • 4 Medical Oncology, University Clinical Centre of the Republic of Srpska - Cancer Centre, 78000 - Banja Luka/BA
  • 5 Medical Oncology, School of Medicine and Pharmacology Sir Charles Gairdner Hospital, 6009 - Nedlands/AU
  • 6 Translational Biology, Zentalis Pharmaceuticals, San Diego/US
  • 7 Clinical Development, Zentalis Pharmaceuticals, New York/US

Resources

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Abstract 562TiP

Background

Ovarian, peritoneal, and fallopian tube cancer are deadly diseases with similar pathological and clinical features. Despite initial therapy with cytoreductive surgery and platinum-based therapy, many patients experience disease relapse either during (refractory) or within 6 months after (resistant) first-line platinum-based therapy. In these patients, various chemotherapies offer clinical activity but none is universally preferred. WEE1 tyrosine kinase is a critical component of G2/M cell cycle checkpoint control and mediates cell cycle arrest by regulating the phosphorylation of cyclin-dependent kinase 1 (CDK1). Inhibition of WEE1 leads to premature mitotic entry, DNA damage and apoptosis induction, and cell death. ZN-c3 is a novel, selective, and orally bioavailable WEE1 inhibitor that has demonstrated significant antitumor activity in nonclinical in vitro and in vivo models. A first-in-human study identified the maximum tolerated dose (MTD) of ZN-c3 when given as monotherapy. Combining ZN-c3 with chemotherapy may inhibit repair of chemotherapy-induced DNA damage and provide therapeutic benefit in this population.

Trial design

This phase 1b, open-label, multicenter study is evaluating the safety, pharmacokinetics, pharmacodynamics, and anti-tumor activity of ZN-c3 in combination with pegylated liposomal doxorubicin, carboplatin, paclitaxel, or gemcitabine. The primary objectives are to determine MTDs and recommended phase 2 doses for each combination by a modified Bayesian continual reassessment method. Subjects are adult women with high-grade serous epithelial ovarian, peritoneal, or fallopian tube carcinoma who have received 1 or 2 prior chemotherapy regimens including platinum-based therapy and are refractory or resistant to platinum-based therapy. Study drug therapy is given in repeated 21- or 28-day cycles until disease progression or unacceptable toxicity. ZN-c3 is taken orally once daily. Chemotherapy is administered per protocol. Pharmacodynamic effects of therapy in tumor tissue and hair follicle samples will be explored. Subject recruitment is ongoing.

Clinical trial identification

NCT04516447

Editorial acknowledgement

Legal entity responsible for the study

Zentalis Pharmaceuticals.

Funding

Zentalis Pharmaceuticals.

Disclosure

A. Pasic: Financial Interests, Personal, Principal Investigator: Zentalis Parmaceuticals. T. Meniawy: Financial Interests, Personal, Advisory Role: Bristol-Myers Squibb; Financial Interests, Personal, Advisory Role: Merck; Financial Interests, Personal, Advisory Role: GlaxoSmithKline; Financial Interests, Institutional, Research Grant: Bristol-Myers Squibb; Financial Interests, Institutional, Research Grant: Merck; Financial Interests, Institutional, Research Grant: GlaxoSmithKline; Financial Interests, Institutional, Research Grant: Novartis; Financial Interests, Institutional, Research Grant: AstraZeneca; Financial Interests, Institutional, Research Grant: Therapim Therapeutics; Financial Interests, Institutional, Research Grant: Beigene; Financial Interests, Institutional, Research Grant: Roche. P.R. de Jong: Financial Interests, Personal, Full or part-time Employment: Zentalis Parmaceuticals; Financial Interests, Personal, Stocks/Shares: Zentalis Parmaceuticals. F. Donate: Financial Interests, Personal, Full or part-time Employment: Zentalis Parmaceuticals; Financial Interests, Personal, Stocks/Shares: Zentalis Parmaceuticals. A.A. Samatar: Financial Interests, Personal, Full or part-time Employment: Zentalis Parmaceuticals; Financial Interests, Personal, Stocks/Shares: Zentalis Parmaceuticals. J. Rodriguez: Financial Interests, Personal, Full or part-time Employment: Zentalis Parmaceuticals; Financial Interests, Personal, Stocks/Shares: Zentalis Parmaceuticals. P. Pultar: Financial Interests, Personal, Full or part-time Employment: Zentalis Parmaceuticals; Financial Interests, Personal, Stocks/Shares: Zentalis Parmaceuticals. D. Voliotis: Financial Interests, Personal, Full or part-time Employment: Zentalis Parmaceuticals; Financial Interests, Personal, Stocks/Shares: Zentalis Parmaceuticals. All other authors have declared no conflicts of interest.

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