Panavance Therapeutics to Present at the Pharma Partnering US Summit 2022

Company to showcase GP-2250 pancreatic and ovarian cancer programs

BERWYN, Pa.–(BUSINESS WIRE)—November 14, 2022 – Panavance Therapeutics Inc. (“Panavance” or the “Company”), a clinical-stage pharmaceutical company advancing the development of a novel oncology therapeutic intended to improve the effectiveness of cancer treatments and quality of life for the patients that receive them, today announced that Greg Bosch, Chairman and CEO of Panavance Therapeutics will present on Thursday, November 17, 2022 at 11:45 AM ET at the Pharma Partnering US Summit 2022 being held in Boston, MA.

Mr. Bosch will provide a Company overview and discuss its lead program, GP-2250, a tumor cell selective and broadly active small molecule with a unique mechanism of action designed to disrupt energy metabolism, resulting in cancer cell death. GP-2250 is currently in a Phase 1 clinical trial with plans to initiate registration directed trials in both pancreatic and ovarian cancers in late 2023.

In addition to the presentation, members of the executive leadership team will be available for in person meetings. To schedule a meeting, please request through the conference’s partnering platform. For more information, please visit the conference website here.

About Panavance Therapeutics
Panavance Therapeutics Inc. is a privately-held, clinical-stage pharmaceutical company developing a novel oncology platform focused on improving the effectiveness of cancer treatments and quality of life for patients. The Company, located in Berwyn, PA was founded in 2021 and continues to be funded by Avensis Pharma AG, a subsidiary of Swiss privately held Ed. Geistlich Söhne AG für Chemische Industrie. Panavance’s lead program, GP-2250, is a tumor cell selective and broadly active small molecule with a unique mechanism of action designed to disrupt energy metabolism, resulting in cancer cell death. GP-2250 is currently in a Phase 1 trial in pancreatic cancer patients. The Company is rapidly advancing towards a pivotal Phase 3 clinical trial, projected to start in the second half of 2023, as a first-line maintenance therapy for pancreatic cancer in non-BRCA mutation patients, a population for which there are no FDA approved agents. Additionally, GP-2250 is being developed for the treatment of ovarian cancer in combination with leading anti-cancer agents based on promising preclinical data. The Company expects to initiate a potential registration directed Phase 1/2 clinical study in ovarian cancer which is expected to start in the second half of 2023. GP-2250 has broad oncology applications and has the potential to be effective in additional indications, including melanoma, squamous cell, breast and colorectal cancers.