Press Releases March 26, 2026

HOOKIPA Pharma Announces Completion of Sale of Oncology Assets to NeoTrail Therapeutics

HOOKIPA Pharma completes sale of key immuno-oncology assets to NeoTrail Therapeutics

By Avery Klein HOOK
HOOKIPA Pharma Announces Completion of Sale of Oncology Assets to NeoTrail Therapeutics
HOOK

HOOKIPA Pharma announced the completion of the sale of its immuno-oncology assets, including the HB-200 and HB-700 development programs, to NeoTrail Therapeutics. The transaction closes the sale agreement signed in January 2026. HB-200 and HB-700 are investigational immunotherapies targeting HPV16 positive cancers and KRAS-mutated cancers respectively. The sale allows HOOKIPA to potentially refocus its strategic priorities while NeoTrail advances these oncology development programs.

Key Points

  • HOOKIPA Pharma sold its immuno-oncology assets HB-200 and HB-700 to NeoTrail Therapeutics.
  • HB-200 is an investigational therapy for HPV16 positive cancers, having received Fast Track and PRIME designations.
  • HB-700 targets KRAS-mutated cancers and is ready for Phase 1 clinical trials with manufacturing completed.
  • The transaction can impact the biotechnology and pharmaceutical sectors, especially companies developing novel cancer immunotherapies.

NEW YORK and VIENNA, March 26, 2026 (GLOBE NEWSWIRE) -- HOOKIPA Pharma Inc. (OTCID: HOOK, “HOOKIPA”, the “Company”) today announced the completion of the sale of its immuno-oncology related assets, consisting primarily of the HB-200 (eseba-vec) and HB-700 development programs, to NeoTrail Therapeutics, Inc. (“NeoTrail”). The purchase price remains undisclosed. The asset purchase agreement was signed on January 28, 2026, and the closing of the transaction occurred on March 20, 2026.

About HB-200
Eseba-vec (also known as HB-200) is an investigational immunotherapeutic agent being evaluated for HPV16 positive cancers. HB-200 alternates the administration of both HB-201 (LCMV) and HB-202 (PICV), collectively referred to as “HB-200,” attenuated viral vectors, which on their own are replicating-based therapeutics expressing a non-oncogenic, but highly immunogenic, E7E6 fusion protein from HPV16. Positive preliminary data from a Phase 2 trial (NCT04180215) of HB-200 in combination with pembrolizumab in patients with recurrent/metastatic HPV16 positive head and neck cancers in the first line setting was presented in November 2024 at the Society for Immunotherapy of Cancer (SITC) Conference. Trial close out activities were completed before the end of 2025. HB-200 received Fast Track Designation from the U.S. Food and Drug Administration and PRIME designation from the European Medicines Agency. HB-200 was developed using HOOKIPA’s proprietary arenavirus platform.

About HB-700
HB-700 is an investigational arenaviral immunotherapy designed to treat KRAS-mutated lung, colorectal, pancreatic and other cancers. HB-700 is a replicating 2-vector therapy that targets the most prevalent KRAS mutations (G12D, G12V, G12R, G12C and G13D) and has the potential to benefit more patients than single mutation inhibitors. HB-700 received Investigational New Drug application clearance from the Food and Drug Administration in April 2024 and is Phase 1 ready, with clinical trial material manufacturing completed.

Availability of Other Information About HOOKIPA
Investors and others should note that HOOKIPA announces material financial information to investors using the Company’s investor relations website, www.ir.hookipapharma.com, OTC Markets filings, press releases, public conference calls and webcasts. HOOKIPA uses these channels, as well as social media, to communicate with investors and the public about the company, and other issues. It is possible that the information HOOKIPA posts on social media could be deemed to be material information. Therefore, investors, the media, and others interested in HOOKIPA are encouraged to review the information on the social media channels listed on the Company’s investor relations website.                


Risks

  • The sale price is undisclosed, creating uncertainty about financial impact for HOOKIPA and investors.
  • Development and regulatory risks remain for HB-200 and HB-700, as they are investigational therapies not yet approved.
  • Transition of programs to NeoTrail introduces operational execution risks affecting clinical progress and market potential.

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