2 Clarke Drive
Suite 100
Cranbury, NJ 08512
© 2024 MJH Life Sciences™ and OncLive - Clinical Oncology News, Cancer Expert Insights. All rights reserved.
A phase 1b trial is investigating the novel GCN2 kinase activator NXP800 in patients with platinum-resistant, ARID1A-mutated ovarian cancer.
NXP800, a novel GCN2 kinase activator, is under further evaluation as a treatment for patients with platinum-resistant, ARID1A-mutated ovarian cancer, in the phase 1b ENGOT-GYN5/NCRI/NXP800-101 trial (GOG-3087; NCT05226507). An overview of the ongoing study was presented at the 2024 SGO Annual Meeting on Women’s Cancer.1
The primary end points of the trial are objective response rate, duration of response, incidence of adverse effects (AEs), and laboratory abnormalities.
“Ovarian cancer is comprised of several subtypes based on histopathology. ARID1A loss is most prevalent in 2 histologic forms of ovarian carcinoma: ovarian clear cell carcinoma (OCCC) and ovarian endometrioid carcinoma,” Susana N. Banerjee, MBBS, MA, PhD, FRCP, and colleagues, wrote in a poster presentation. Banerjee is a consultant medical oncologist at The Royal Marsden NHS Foundation Trust and team leader in Women’s Cancers at The Institute of Cancer Research in London.
NXP800 is an antineoplastic, oral, small molecule activator of the GCN2 kinase. In preclinical models, it displayed robust antitumor activity, including in ARID1A-mutated ovarian carcinoma, endometrial carcinoma, and cholangiocarcinoma.
Previously reported data from the phase 1a portion of the trial showed that the most common treatment-emergent AEs in patients with various types of non-target, advanced solid tumors, consisted of vomiting, nausea, diarrhea, fatigue, decreased appetite, and weight loss. Common lab abnormalities included transient changes in platelets, liver enzymes, and red blood cells. No drug-related grade 4 or grade 5 AEs were reported.2
Based on initial pharmacokinetic and pharmacodynamic data from phase 1a, 50 mg of NXP800 per day and 75 mg of NXP800 per day were selected as the doses for phase 1b.
Phase 1b is enrolling patients with clear cell ovarian carcinoma or endometrioid ovarian carcinoma harboring pathogenic ARID1A mutations, as determined by DNA-based next-generation sequencing. Patients are required to have measurable disease per RECIST v1.1 criteria and must have received at least 1 and no more than 5 prior lines of systemic therapy, including at least 1 line of therapy that contained bevacizumab (Avastin).1 However, prior bevacizumab is not required for patients who did not receive the agent due to recto-sigmoid involvement by pelvic examination, bowel involvement on CT scan, or clinical symptoms of bowel obstruction.
The trial is excluding patients whose disease did not respond to, or has progressed during or within 4 weeks of, the last dose of first-line, platinum-containing chemotherapy.
Pharmacokinetics parameters will serve as a secondary end point. Change in expression of CHAC1, ATF3, ATF4, HSP27 and other proteins at RNA or protein level before and after treatment with NXP800 is a key exploratory end point.
The phase 1b portion of the trial is currently open for enrollment in the United Kingdom and the United States.
In December 2022, the FDA granted fast track designation to NXP800 for the treatment of patients with platinum-resistant, ARID1A-mutated ovarian cancer.3 Additionally, in August 2023, the regulatory agency granted an orphan drug designation to NXP800 for the treatment of patients with cholangiocarcinoma.4