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Arvinas (ARVN) pipeline and stated timing

Pipeline at a glance

ProgramEventStageStated timingFiling
ARV-102/data readoutPhase 1fourth quarter of 202610-Q ·
ARV-393Topline/data readoutPhase 1second half of 202610-Q ·
ARV-806Topline/data readoutPhase 1second half of 2026EX-99.1 ·

Source: ORION, orionbiotechai.com/company/ARVN, data as of Oct 13, 2026
https://www.orionbiotechai.com/company/ARVN

Nearest upcoming stated timing: ARV-102 · Topline/data readout · fourth quarter of 2026

SEC sources last checked .

Programs and stated timing

○ Quote matched to filing (not yet reviewed by founder) · ✓ Checked by founder.

Topline/data readoutfourth quarter of 2026

Stage: Phase 1SEC filing · “Phase 1”

Public float: $469,000,000 · as of · SEC filing

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

10-Q · Filed · Last checked

Source details

Accession 0001628280-26-052554

Topline/data readoutsecond half of 2026

Stage: Phase 1SEC filing · “Phase 1”

Public float: $469,000,000 · as of · SEC filing

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

10-Q · Filed · Last checked

Source details

Accession 0001628280-26-052554

Topline/data readoutsecond half of 2026

Stage: Phase 1SEC filing · “Phase 1”

Public float: $469,000,000 · as of · SEC filing

KRAS G12D mutations. ◦ Reiterated plan to share initial data from the Phase 1 monotherapy dose escalation clinical trial in the second half of 2026

EX-99.1 · Filed · Last checked

Source details

Accession 0001628280-26-052139

How this date was described over time

Company periods and sentences are quoted as written. A matching disclosure uses the SEC filing date for the same program and event type. As of .

Program / eventStated period and SEC wordingDisclosure in stated period
ARV-102Clinical resultsfourth quarter of 2026
“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”

Filed · 10-Q

Still within period

As of Oct 19, 2026

ARV-393Clinical resultssecond half of 2026
“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”

Filed · 10-Q

Still within period

As of Oct 19, 2026

ARV-806Clinical resultssecond half of 2026
“KRAS G12D mutations. ◦ Reiterated plan to share initial data from the Phase 1 monotherapy dose escalation clinical trial in the second half of 2026”

Filed · EX-99.1

Still within period

As of Oct 19, 2026

ARV-102Clinical resultssecond half of 2026
“additional biomarker data from the Phase 1 clinical trial in patients with PD in the second half of 2026”

Filed · 10-Q

Not compared

ORION has no confirmed start and end dates for this wording, so it is not compared with filings.

ARV-806Clinical results2026
“initial clinical data in patients with solid tumors harboring KRAS G12D mutations in 2026”

Filed · 10-Q

Not compared

ORION has no confirmed start and end dates for this wording, so it is not compared with filings.

ARV-806Clinical results2026
“initial clinical data i n patients with solid tumors harboring KRAS G12D mutations in 2026”

Filed · 10-K

Not compared

ORION has no confirmed start and end dates for this wording, so it is not compared with filings.

“Not compared” means ORION has not matched this wording against a complete set of SEC filings for its period. It says nothing either way about whether a matching filing exists. Wording without exact dates is not given calendar dates.

Retained company announcements

Historical summaries and source dates are retained separately from the SEC timing quotes above. Earlier publications were collected retrospectively.

Historical catalog checked .

No historical announcement trail is retained for this company in this catalog.

Selected registry record

ARV-806 · NCT07023731

Condition in the selected registry record
KRAS G12D Mutation
Phase in the selected registry record
Phase 1 / Phase 2
Identity checked

Original ClinicalTrials.gov record · Open the selected study

Retained company–study identity sources

Scope of retained company and registry evidence

These are selected linked records and dated source metadata, not a live registry recheck or the company’s full pipeline. Company announcements and the selected registry study are separate evidence sets. No stage or event timing is borrowed between them.

Coverage and identity checks

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Reading these records

First stated window
The timing wording in the earliest company statement located within the sources checked, quoted as written (for example “2H 2026”). An earlier statement may exist outside those sources.
Disclosure date
The date of the filing or company release that disclosed the readout. “None found” means no such disclosure was located in the sources checked. SEC filings were searched through the “SEC filings searched through” date shown.
1H, 2H, 1Q–4Q
First or second half, or first to fourth quarter, of the year named, as the company wrote it. Equivalent notations are compared together; the original wording stays visible.
SEC original
The filing as published on the SEC EDGAR system. “Company original” is the release on the company's own investor site.
Status
One of seven labels set by founder review of the original filings. Definitions: Methodology.

See ARVN in the calendar · Review labels and methodology

Topline results are the main summary results of a clinical trial, released before the full data.