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Arvinas to Present at Jefferies Global Healthcare Conference

Key Takeaway: Arvinas, Inc. will participate in a fireside chat at the Jefferies Global Healthcare Conference on November 18. The company is known for its innovative protein degradation therapies and has multiple investigational drugs in clinical trials. Arvinas recently achieved FDA approval for its first PROTAC drug, developed in partnership with Pfizer.

Market Sentiment Analysis

POSITIVE FACTORS

  • Arvinas is pioneering new drug therapies.
  • The company has FDA-approved PROTAC technology.
  • Multiple investigational drugs are in clinical development.
  • Management will present at a significant healthcare conference.

BiopharmaWatch Analysis

From our catalyst data and publicly available data · not financial advice
Best trade, last catalyst
+9%
120-day peak, hindsight
Typical move
3.4%
average across 15 past catalysts
Cash runway
~161 mo
Low dilution risk
Lead asset
ARV-806
Phase 2 · KRAS G12D Mutation

Full Press Release Details

NEW HAVEN, Conn., Nov. 11, 2026 (GLOBE NEWSWIRE) -- Arvinas, Inc. (Nasdaq: ARVN), a clinical-stage biotechnology company creating a new class of drugs based on targeted protein degradation, today announced that management will participate in a fireside chat at the Jefferies Global Healthcare Conference on Wednesday, November 18 at 9:00 a.m. GMT/4:00 a.m. EST.
A live audio webcast of the presentation will be available here and under “Events and Presentations” on the Investors and Media section of the Company’s website.

About Arvinas

Arvinas (Nasdaq: ARVN) is a clinical-stage biotechnology company dedicated to improving the lives of patients suffering from debilitating and life-threatening diseases. Through its PROteolysis TArgeting Chimera (PROTAC) protein degrader platform, Arvinas is pioneering the development of protein degradation therapies designed to harness the body’s natural protein disposal system to selectively and efficiently degrade and remove disease-causing proteins. Arvinas, with its partner Pfizer, developed the first U.S. Food and Drug Administration (FDA)-approved PROTAC, a type of heterobifunctional protein degrader, which has been outlicensed to Rigel Pharmaceuticals, Inc. for exclusive global development, manufacturing, and commercialization.
Arvinas is currently progressing multiple investigational drugs through clinical development programs, including ARV-393, targeting BCL6 for relapsed/refractory non-Hodgkin Lymphoma; ARV-102, targeting LRRK2 for neurodegenerative disorders; ARV-027, targeting the polyglutamine-expanded androgen receptor, or polyQ-AR, in skeletal muscle for spinal-bulbar muscular atrophy, also known as Kennedy’s disease; and ARV-6723, targeting HPK1 for advanced solid tumors. Arvinas has also advanced ARV-806, targeting KRAS G12D for solid tumors, in the clinic, and previously announced plans to seek an out-licensing agreement for any additional clinical trials of ARV-806, including dose expansion or combination clinical trials. Arvinas is headquartered in New Haven, Connecticut. For more information about Arvinas, visit www.arvinas.com and connect on LinkedIn and X.

Contacts Investors: Jeff Boyle +1 (347) 247-5089 Jeff.Boyle@arvinas.com

Media: Kirsten Owens +1 (203) 584-0307 Kirsten.Owens@arvinas.com

Frequently Asked Questions

When is Arvinas presenting at the conference?

Arvinas will present on November 18 at 9:00 a.m. GMT.

What is the focus of Arvinas' drug development?

Arvinas focuses on targeted protein degradation therapies.

What is PROTAC technology?

PROTAC is a platform for developing protein degradation therapies.

Who is Arvinas' partner for PROTAC development?

Arvinas partnered with Pfizer for PROTAC development.

Last updated: Nov 11, 2026