Biopharma Transcript

Arvinas, Inc. ARVN

Nasdaq · Phase 1 · oncology · small molecule · EDGAR · Updated Nov 5, 2026

Arvinas, Inc. (Nasdaq: ARVN) is an oncology drug developer. Its lead program, ARV-6723, is in Phase 1 for advanced solid tumors.

Upcoming catalysts

No catalyst is dated to the next 30 days or to an FDA action date.

Pipeline

ProgramIndicationModalityStage
VEPPANU (vepdegestrant)ER+/HER2-, ESR1-mutated advanced or metastatic breast cancersmall moleculeApproved
Luxdegalutamide (ARV-766)metastatic castration-resistant prostate cancersmall moleculePhase 3
ARV-393relapsed/refractory NHL (B-cell and T-cell lymphomas)small moleculePhase 1
ARV-027spinal bulbar muscular atrophy (SBMA)small moleculePhase 1
ARV-6723advanced solid tumorssmall moleculePhase 1
ARV-102Parkinson's disease, PSPsmall moleculePhase 1
ARV-806advanced solid tumors with KRAS G12D mutationssmall moleculePhase 1

Recent results and decisions

  1. Nov 3, 2026
    started Arvinas initiated dosing in a Phase 1/2 trial of ARV-6723, an oral PROTAC HPK1 degrader, for advanced solid tumors.Initiated dosing of patients in the monotherapy cohort of the Phase 1/2 clinical trial (ClinicalTrials.gov Identifier: NCT07749586) of ARV-6723, Arvinas' first immuno-oncology degrader. Filing
  2. Nov 3, 2026
    positive ARV-102 Phase 1 trial showed improved eye movement and biomarker changes in patients with Parkinson's disease.Data showed improvements in an objective measure of impaired eye movement associated with Parkinson's disease. Changes in oculomotor function correlated with reductions in LRRK2 cerebrospinal fluid biomarkers and changes in synaptic biomarkers. Filing
  3. Nov 3, 2026
    n/a Arvinas plans to submit a clinical trial application for ARV-102 in PSP in the EU in Q4 2026 and in the UK in Q1 2027.Submit clinical CTA to initiate Phase 1b trial in patients with PSP (EU 4Q 2026; UK 1Q 2027). Filing

1 more on record.

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