Press Releases May 29, 2026 04:01 PM

Arvinas to Present at Jefferies Global Healthcare Conference

Arvinas to participate in Jefferies Global Healthcare Conference fireside chat highlighting clinical pipeline and recent developments.

By Priya Menon ARVN

Arvinas, Inc., a clinical-stage biotech company specializing in targeted protein degradation therapies, announced its management will present at the Jefferies Global Healthcare Conference. The presentation will cover its PROTAC platform, FDA-approved drug VEPPANU™, and several investigational drugs targeting neurodegenerative diseases, cancers, and rare conditions. The company also disclosed an ongoing transaction with Rigel Pharmaceuticals for exclusive global rights to VEPPANU™, pending regulatory approvals.

Arvinas to Present at Jefferies Global Healthcare Conference
ARVN

Key Points

  • Arvinas will participate in a fireside chat at the Jefferies Global Healthcare Conference on June 3, 2026.
  • The company highlights its FDA-approved PROTAC drug VEPPANU™ for treating advanced breast cancer and its multiple clinical-stage drug candidates targeting serious diseases.
  • Announcement of a transaction with Rigel Pharmaceuticals for exclusive global rights to VEPPANU™, subject to regulatory approvals.
  • Impacted sectors include biotechnology, pharmaceuticals, healthcare, oncology, and neurology markets.

NEW HAVEN, Conn., May 29, 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, June 3 at 9:55 a.m. ET.

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 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 Inc., 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 and Pfizer have entered into a transaction with Rigel Pharmaceuticals, Inc. for the exclusive global rights of VEPPANU; closing of the transaction is subject to the parties’ receipt of any necessary consents or approvals, including the expiration or termination of the waiting period under the Hart-Scott-Rodino Antitrust Improvements Act of 1976, as amended.

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 and colorectal cancers; ARV-393, targeting BCL6 for relapsed/refractory non-Hodgkin Lymphoma; ARV-027, targeting the polyglutamine-expanded androgen receptor, or polyQ-AR, in skeletal muscle for the treatment of Spinal-Bulbar Muscular Atrophy, also known as Kennedy’s disease; and vepdegestrant, targeting the estrogen receptor for patients with locally advanced or metastatic ER+/HER2- breast cancer. Arvinas is headquartered in New Haven, Connecticut. For more information about Arvinas, visit www.arvinas.com and connect on LinkedIn and X.

VEPPANU is a trademark of Arvinas Operations, Inc.

Contacts
Investors:
Jeff Boyle
+1 (347) 247-5089
[email protected]

Media:
Alyssa Kuciunas
+1 (331) 481-3751
[email protected]


Risks

  • Closing of the transaction with Rigel Pharmaceuticals is subject to necessary consents and regulatory approvals, which may delay or prevent completion.
  • Clinical development programs carry typical biotech risks such as trial failures, regulatory delays, or funding challenges.
  • Market acceptance and commercial success of PROTAC-based therapies remain uncertain given the novel nature of the technology, impacting biotech and pharma sectors.

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