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Arvinas to Report Third Quarter 2026 Financial Results on November 3, 2026

Key Takeaway: Arvinas, Inc. will report its third quarter 2026 financial results on November 3, 2026. The live webcast will begin at 8:00 a.m. ET, accessible via the investor page on their website. The company is known for its innovative protein degradation therapies and has several investigational drugs in clinical development.

Market Sentiment Analysis

POSITIVE FACTORS

  • Arvinas is advancing multiple investigational drugs.
  • The company has developed the first FDA-approved PROTAC.
  • Management will provide a corporate update during the webcast.

BiopharmaWatch Analysis

From our catalyst data and publicly available data · not financial advice
Best trade, last catalyst
+11%
120-day peak, hindsight
Typical move
3.1%
average across 14 past catalysts
Cash runway
~33 mo
Low dilution risk
Lead asset
ARV-110
Phase 1 · Prostate Cancer Metastatic

Full Press Release Details

NEW HAVEN, Conn., Oct. 27, 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 review third quarter 2026 financial results and provide a corporate update during a live webcast on Tuesday, November 3, 2026 at 8:00 a.m. ET.
The webcast can be accessed under “Events and Presentations” on the investor page of the Arvinas website. A replay of the webcast will be available on the Arvinas website at www.arvinas.com following the completion of the event.

About Arvina

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 will Arvinas report its Q3 2026 financial results?

Arvinas will report its Q3 2026 financial results on November 3, 2026.

How can I access the Arvinas webcast?

The webcast can be accessed on the investor page of the Arvinas website.

What is the focus of Arvinas' drug development?

Arvinas focuses on targeted protein degradation therapies for serious diseases.

What is a PROTAC?

A PROTAC is a type of heterobifunctional protein degrader developed by Arvinas.

Last updated: Oct 27, 2026