Arvinas
Market cap $420M 65.5M shares (10-Q, Oct 30, 2026) × $6.41 close Nov 6, 2026
Most recent annual filing: 2026-02-24
- ARV-393 Ph1 interim2H 2026ARV-393 Ph1 interim, 2H 2026, notable
- ARV-806 KRAS readout4Q 2026ARV-806 KRAS readout, 4Q 2026, notable
- ARV-027 polyQ-AR readout1H 2027ARV-027 polyQ-AR readout, 1H 2027, notable
- ARV-102 Ph1 start2027ARV-102 Ph1 start, 2027, routine
Bar width shows how precise the guidance is — a pin is a stated date, a wide band a six-month window. Deeper blue means more of the thesis rides on the event; it is not a view on the stock.
Pipeline (10 active programs)
ARV-102
ARV-393
ARV-027
ARV-6723
luxdegalutamide
ARV-766pan-KRAS degrader
- Undisclosed indication
ARV-806
Technology platforms
PROTAC Discovery Engine
Integrated suite of tools and expertise for discovery and optimization of PROTAC targeted protein degraders, including E3KnowledgeBase, ANGLE linker evolution, LEAP library format, PROTACify ML modeling, proteomics capabilities, and PIVOT PK/PD tool. Focus areas: oncology and neurology, including historically undruggable intracellular targets such as transcription factors, scaffolding proteins, and oncoproteins.
PROTAC
Proteolysis Targeting Chimera (PROTAC) protein degrader platform; harnesses the body's ubiquitin-proteasome system to degrade disease-causing proteins; applications in oncology (AR, ER, BCL6, HPK1) and neurology (LRRK2, polyQ-AR); enables oral delivery and blood-brain barrier penetration
Targets: AR, ESR1, BCL6, HPK1, LRRK2, polyQ-AR
PROTAC protein degrader platform
PROteolysis TArgeting Chimera (PROTAC) protein degrader platform that harnesses the body's natural protein disposal system to selectively and efficiently degrade disease-causing intracellular proteins, including historically undruggable targets; applied across oncology and neurology indications.
PROTAC · Pfizer
PROteolysis TArgeting Chimera protein degrader platform — harnesses the body's natural protein disposal system (ubiquitin-proteasome system) to selectively degrade disease-causing proteins; applied across oncology and neurology indications
Discontinued (1)
- bavdegalutamide — Metastatic Castration-Resistant Prostate Cancer · deprioritized in favor of luxdegalutamide; clinical trials completed Q2 2025
Capital (as filed)
- Cash
- $88.0M cash and cash equivalents · Sep 30, 2026 (10-Q)
- Short-term investments
- $470M Sep 30, 2026
- Operating cash flow
- −$10.4M quarter Jun 30, 2026 → Sep 30, 2026, year-to-date difference (10-Q)
- As stated in coverage
- $559M cash, runway 2H 2028 per the update of Nov 3, 2026 — the company's own words as read there, not the filed figure
Offering documents (1)
- 2026-11-03 S-3 · Shelf registration up to $200M aggregate
Cash, investments and operating cash flow are the company's own XBRL facts as filed with the SEC, each shown with its period end and tag. As-stated figures come from the company's own words as read in Biotech Distilled coverage, dated, and routinely count securities and planned financing that a balance sheet does not. Offering rows are the SEC cover pages as filed. Not investment advice. Figures as of Nov 7, 2026.
Biotech Distilled coverage (8)
- 2026-11-04 UPDATE: Arvinas (ARVN) - The FDA Answered, and Arvinas Is Going Around It 🔒 Paid
- 2026-10-08 UPDATE: Arvinas (ARVN) - ARV-102 Moves the Eyes, Not Yet the Needle 🔒 Paid
- 2026-08-04 UPDATE: Arvinas (ARVN) - The Catalyst Window Just Slid a Year Right 🔒 Paid
- 2026-06-22 UPDATE: Arvinas (ARVN) - The CMO Walks Three Weeks Before the Catalyst Window Opens 🔒 Paid
- 2026-06-02 UPDATE: Arvinas (ARVN) - The KRAS Asset Gets the Novartis Treatment
- 2026-05-12 UPDATE: Arvinas (ARVN) - The Partner Lands. The Tape Yawns. 🔒 Paid
- 2026-05-02 UPDATE: Arvinas (ARVN) - The First PROTAC Crosses the Finish Line 🔒 Paid
- 2026-04-10 Arvinas (ARVN) - Scientific Deep Dive for Vepdegestrant, Luxdegalutamide, and Pipeline Products 🔒 Paid
Articles open on Substack. Some are subscriber-only; those marked ★ Distilled Pro are for Distilled Pro members.
Verdict history (8 calls)
Every verdict Biotech Distilled has published on Arvinas, oldest first — the full history, never a selection. How calls are scored: the track record.
- 2026-04-10 Watch Arvinas (ARVN) - Scientific Deep Dive for Vepdegestrant, Luxdegalutamide, and Pipeline Products The PROTAC science is compelling but the commercial setup for vepdegestrant is muddy with no partner named, making it too risky to go long yet.
- 2026-05-02 Speculative buy speculative UPDATE: Arvinas (ARVN) - The First PROTAC Crosses the Finish Line FDA approval of the first-ever PROTAC eliminates modality risk and partially de-risks the platform, warranting a small speculative position while awaiting a commercial partner announcement.
- 2026-05-12 Buy core UPDATE: Arvinas (ARVN) - The Partner Lands. The Tape Yawns. Both major overhangs — FDA approval and commercial partner — are now resolved, and the pipeline is quietly delivering strong biomarker signals, justifying an upgrade to BUY despite Rigel being a mid-tier partner.
- 2026-06-02 Speculative buy speculative UPDATE: Arvinas (ARVN) - The KRAS Asset Gets the Novartis Treatment ARV-806 being punted to a future out-licensing partner narrows the wholly-owned pipeline thesis and concentrates bets on ARV-102 and ARV-393, warranting a downgrade to speculative.
- 2026-06-22 Watch UPDATE: Arvinas (ARVN) - The CMO Walks Three Weeks Before the Catalyst Window Opens A CMO departure three weeks before the catalyst window, stacked on top of a CEO transition and pipeline narrowing, raises execution risk enough to step back to the sidelines pending CMO succession and readouts.
- 2026-08-04 Speculative buy speculative UPDATE: Arvinas (ARVN) - The Catalyst Window Just Slid a Year Right The ARV-102 PSP clinical hold is procedural rather than a safety break, the balance sheet funds operations into 2H 2028 with no dilution gap, and the science thesis is intact — warranting a modest re-entry despite the one-year calendar slip.
- 2026-10-08 Speculative buy speculative UPDATE: Arvinas (ARVN) - ARV-102 Moves the Eyes, Not Yet the Needle ARV-102 produced a dose-dependent, placebo-controlled eye-movement signal in 24 PD patients, modestly lifting the scientific floor, but the PSP clinical hold remains unresolved so conviction does not scale.
- 2026-11-04 Watch UPDATE: Arvinas (ARVN) - The FDA Answered, and Arvinas Is Going Around It The U.S. PSP IND remains on hold after the tox package was submitted, ARV-806 has dropped off the pipeline deck, a second Big Pharma partner has exited, and a fresh $200M ATM prospectus at sub-cash prices raises dilution risk — warranting a return to the sidelines.
- Long call · opened May 4, 2026 at $10.78 · closed Jun 23, 2026 (downgraded to WATCH from long) at $8.14 · -24.5% vs XBI +10.1%
- Long call · opened Aug 5, 2026 at $8.40 · closed Nov 4, 2026 (downgraded to WATCH from long) at $7.42 · -11.7% vs XBI +4.0%
Every verdict Biotech Distilled has published on this company, in order, with the post it came from — the full history, never a selection. Position figures are the same ones shown on /track-record, computed by the same method. Editorial opinion, not investment advice.
Timing, in the company's words (9 quotes from 4 filings)
Sentences quoted verbatim from the company's SEC filings, newest filing first. Each sits under the filing it appeared in; the "matched to" tag names the calendar row it was read for.
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“Enrollment in this clinical trial is currently ongoing, and we plan to share initial data from this combination cohort of ARV-393 with glofitamab in patients with DLBCL in mid-2027.”
matched to ARV-393 · interim data · read as mid-2027 -
“In the second quarter of 2026, we announced that we had completed dose escalation enrollment of the Phase 1 clinical trial, and we plan to share clinical data from this Phase 1 monotherapy dose escalation clinical trial in the fourth quarter of 2026.”
matched to ARV-806 (KRAS G12D) · readout other · read as fourth quarter of 2026
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“Submit clinical CTA to initiate Phase 1b trial in patients with PSP (EU 4Q 2026; UK 1Q 2027).”
matched to ARV-027 (polyQ-AR) · readout other · read as 4Q 2026
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“In the second quarter of 2026, we completed the single-ascending dose cohorts in the first-in-human Phase 1 clinical trial in healthy volunteers and, in the third quarter of 2026, we initiated enrollment in the multiple dose cohorts in the Phase 1 clinical trial in healthy volunteers.”
matched to ARV-027 (polyQ-AR) · readout other · read as third quarter of 2026 -
“We plan to share clinical data from the early monotherapy cohorts in the ongoing Phase 1 dose escalation clinical trial of ARV-393 in patients with relapsed/refractory NHL at a medical congress in the second half of 2026.”
matched to ARV-393 · interim data · read as second half of 2026 -
“We are planning to complete this Phase 1 monotherapy dose escalation clinical trial and share clinical data in the second half of 2026.”
matched to ARV-806 (KRAS G12D) · readout other · read as second half of 2026
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“We plan to share additional biomarker data from the Phase 1 clinical trial in patients with PD at the International Congress on Parkinson’s Disease and Movement Disorders in the fourth quarter of 2026.”
matched to ARV-102 · trial initiation · read as fourth quarter of 2026 -
“Initiate enrollment of the Phase 1 clinical trial in patients with advanced solid tumors (3Q 2026).”
matched to ARV-6723 (HPK1) · trial initiation · read as 3Q 2026 -
“We are planning to complete this Phase 1 monotherapy dose escalation clinical trial and share clinical data in the second half of 2026.”
matched to ARV-806 (KRAS G12D) · Initial clinical data in patients with solid tumors · read as second half of 2026
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Timing sentences quoted from the company's own SEC filings, each under the filing it appeared in. The 'matched to' tag is the calendar row the sentence was read for; the filing is the source. Not investment advice.
Filings & releases (32)
SEC filings from EDGAR and press releases captured from the company's investor-relations site, newest first. Releases captured from May 5, 2026; filings from March 2026. Summaries come from the BD update that read the document; "BD extracted" counts point at the pipeline table above. All companies →
- Nov 4, 2026ReleaseArvinas to Present Preliminary Clinical Data from Early Monotherapy Dose Escalation Cohorts in the Phase 1 Trial for ARV-393 (Zaloblideg), a PROTAC BCL6 Degrader, at the 2026 American Society of Hemat
- Nov 3, 2026S-3Shelf registration→ BD updateSummary on the 8-K
- Nov 3, 2026ReleaseArvinas Reports Third Quarter 2026 Financial Results and Provides Corporate Update→ BD updateSummary on the 8-K
- Nov 3, 20268-KCurrent report: results of operations, Reg FD disclosure · EX-99.1→ BD updateQ3 earnings confirm ARV-6723 is now dosing patients, ARV-393 data lands at ASH in December, and $558.9M cash holds the fort — but the stock is at $7.09, the CMO seat is still empty, and a fresh $400M shelf registration raises dilution awareness heading into the catalyst window.
- Nov 3, 202610-QQuarterly report→ BD updateSummary on the 8-K
- Oct 27, 2026ReleaseArvinas to Report Third Quarter 2026 Financial Results on November 3, 2026
- Oct 27, 2026ReleaseArvinas Announces Return of Early Career Researcher Award to Recognize Innovation in Targeted Protein Degradation
- Oct 7, 2026ReleaseArvinas Shares Novel Oculomotor and Biomarker Data from Phase 1 Clinical Trial of ARV-102 in Patients with Parkinson’s Disease→ BD updateThe final ARV-102 Phase 1 data at MDS 2026 deliver the closest thing to a clinical signal this trial was designed to produce: dose-dependent improvements in an objective eye-movement measure of Parkinson's severity, correlated with CSF LRRK2 degradation — expanding the biomarker case for the PSP program still waiting on FDA clearance.BD extracted 1 program update from this document → ARVN pipeline
- Oct 1, 2026ReleaseArvinas to Present Novel Biomarker Data from the Phase 1 Clinical Trial for ARV-102, a PROTAC LRRK2 Degrader, at the 2026 International Congress of Parkinson’s Disease and Movement Disorders®ARV-102's Phase 1 Parkinson's data lands at MDS as a late-breaking oral on October 7 — and it includes oculomotor biomarkers that haven't appeared in any prior Arvinas update, suggesting the dataset has grown since the August hold announcement.BD extracted 1 program update from this document → ARVN pipeline
- Sep 28, 2026ReleaseArvinas Announces First Patient Dosed in Phase 1/2 Clinical Trial of ARV-6723, the Company’s First Immuno-Oncology CandidateARV-6723, Arvinas's first immuno-oncology PROTAC targeting HPK1, has dosed its first patient — the one 2H 2026 catalyst that actually stayed on schedule after the ARV-102 PSP hold pushed the rest of the wholly-owned pipeline into 2027.
- Sep 3, 2026ReleaseArvinas to Participate in Upcoming Investor Conferences
- Aug 4, 2026ReleaseArvinas Reports Second Quarter 2026 Financial Results and Provides Corporate UpdateBD extracted 2 program updates from this document → ARVN pipeline
- Aug 4, 20268-KCurrent report: results of operations · EX-99.1
- Aug 4, 202610-QQuarterly report
- Jul 28, 2026ReleaseArvinas to Report Second Quarter 2026 Financial Results on August 4, 2026
- Jun 25, 20268-KCurrent report: shareholder vote
- Jun 22, 20268-KCurrent report: officer / director change
- Jun 16, 20268-KCurrent report: other events
- Jun 4, 2026ReleaseArvinas Joins The Michael J. Fox Foundation’s LITE and PPMI Programs to Advance New Therapies Targeting LRRK2 for Parkinson’s Disease
- Jun 2, 20268-KCurrent report: Reg FD disclosure, other events · EX-99.1
- May 29, 2026ReleaseArvinas to Present at Jefferies Global Healthcare Conference
- May 18, 2026ReleaseArvinas Employees Give Back During Company-wide Impact Day
- May 12, 2026ReleaseArvinas and Pfizer Enter into a Transaction with Rigel Pharmaceuticals for the Exclusive Global Rights of VEPPANU (vepdegestrant)
- May 12, 2026ReleaseArvinas Reports First Quarter 2026 Financial Results and Provides Corporate Update
- May 12, 20268-KCurrent report: results of operations · EX-99.1
- May 12, 20268-KCurrent report: material agreement, Reg FD disclosure · EX-99.1
- May 11, 202610-QQuarterly report
- May 5, 2026ReleaseArvinas to Report First Quarter 2026 Financial Results on May 12, 2026
- May 1, 20268-KCurrent report: Reg FD disclosure, other events · EX-99.1
- Apr 29, 2026DEFA14AProxy soliciting material
- Apr 29, 2026DEF 14AProxy statement
- Mar 18, 20268-KCurrent report: Reg FD disclosure, other events · EX-99.1
6 more filings (13G holder notices, S-8, proxy material, SEC correspondence …)
- Sep 28, 2026S-8Employee plan registrationSummary on the release
- Aug 31, 2026S-8Employee plan registration
- Aug 14, 2026SCHEDULE 13G/A13G amendment
- Apr 29, 2026ARSAnnual report to shareholders
- Apr 28, 2026SCHEDULE 13GPassive >5% holder (13G)
- Mar 26, 2026SCHEDULE 13G/A13G amendment