Imunon 11.1 Month Increase in Overall Survival with Ovarian Cancer Treatment

 

• Phase 2 OVATION 2 Study of IMNN-001 administered with standard-of-care chemotherapy as first-line treatment demonstrates a hazard ratio of 0.74 in overall survival (OS) in the intent-to-treat patient population compared with the standard-of-care control arm
• OS was extended by 15.7 months in patients receiving three or more doses of IMNN-001 in the 17-dose protocol
• Patients also receiving maintenance PARP inhibitor therapy demonstrated an OS hazard ratio of 0.41 in the IMNN-001 trial arm with median OS not yet reached at the time of data lock
• Robust and durable benefit of IMNN-001 observed in OS supported by a three-month improvement in the primary endpoint of progression-free survival (PFS)
• IMUNON expects to initiate a registrational study in Q1 2025

Conference call begins today at 8:30 a.m. Eastern time

IMUNON is hosting a conference call at 8:30 a.m. Eastern time today to discuss OVATION 2 Study results, next steps and to answer questions. Dr. Thaker will be joining management on the call. To participate in the conference call, please dial 833-816-1132 (Toll-Free/North America) or 412-317-0711 (International/Toll) and ask for the IMUNON call. A live webcast of the call will be available here.

Participants are encouraged to preregister for the call here.

The call will be archived for replay through August 13, 2024. The replay can be accessed at 877-344-7529 (U.S. Toll-Free), 855-669-9658 (Canada Toll-Free) or 412-317-0088 (International Toll), using the replay access code 7783601. A webcast of the call will be available here for 90 days.

https://www.globenewswire.com/news-release/2024/07/30/2920936/0/en/IMUNON-Announces-11-1-Month-Increase-in-Overall-Survival-in-Patients-with-Newly-Diagnosed-Advanced-Ovarian-Cancer-Treated-with-IMNN-001.html