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Arvinas to Report First Quarter 2026 Financial Results on May 12, 2026

Key Takeaway: Arvinas, Inc. will report its first quarter 2026 financial results and provide a corporate update on May 12, 2026. The live webcast will begin at 8:00 a.m. ET and will be accessible on the company's investor page. Arvinas is known for its innovative protein degradation therapies and has made significant advancements in treating various cancers and neurodegenerative disorders.

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.

Full Press Release Details

NEW HAVEN, Conn., May 05, 2026 (GLOBE NEWSWIRE) -- Arvinas, Inc. (Nasdaq: ARVN), a biotechnology company working to create a new class of drugs based on targeted protein degradation, today announced that management will review first quarter 2026 financial results and provide a corporate update during a live webcast on Tuesday, May 12, 2026 at 8:00 a.m. ET.
The webcast can be accessed under “Events and Presentations” on theinvestor pageof the Arvinas website. A replay of the webcast will be available on the Arvinas website atwww.arvinas.comfollowing the completion of the event.

About Arvinas

Arvinas (Nasdaq: ARVN) is a biotechnology company dedicated to improving the lives of patients suffering from debilitating and life-threatening diseases. Through its PROTAC (PROteolysis TArgeting Chimera) 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-and-only U.S. Food and Drug Administration (FDA) approved PROTAC, a type of heterobifunctional protein degrader, VEPPANU (vepdegestrant), for the treatment of adults with estrogen receptor-positive (ER+)/human epidermal growth factor receptor 2-negative (HER2-), ESR1-mutated advanced or metastatic breast cancer, as detected by an FDA-authorized test, with disease progression following at least one line of endocrine therapy.
Arvinas is currently progressing multiple investigational drugs through clinical development programs, including ARV-102, targeting LRRK2 for neurodegenerative disorders; ARV-806, targeting KRAS G12D for mutated cancers, including pancreatic, colorectal, and non-small cell lung cancers; ARV-393, targeting BCL6 for relapsed/refractory non-Hodgkin Lymphoma; and ARV-027, targeting the polyglutamine-expanded androgen receptor, or polyQ-AR, in skeletal muscle. Arvinas is headquartered in New Haven, Connecticut.For more information about Arvinas, visitwww.arvinas.comand connect onLinkedInandX.

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

Media:Alyssa Kuciunas+1 (331) 481-3751alyssa.kuciunas-c@arvinas.com

Frequently Asked Questions

When will Arvinas report its Q1 2026 financial results?

Arvinas will report its Q1 2026 financial results on May 12, 2026.

How can I access the Arvinas webcast?

The webcast can be accessed on the 'Events and Presentations' section of the Arvinas investor page.

What is the focus of Arvinas' drug development?

Arvinas focuses on developing therapies based on targeted protein degradation.

What is the significance of VEPPANU?

VEPPANU is the first FDA-approved PROTAC for treating certain types of breast cancer.

Last updated: May 5, 2026