Phase 3 topline

Primary completion of ABTECT - Maintenance

AAVXF · Abivax S.A. · ABX464 · Ulcerative Colitis

Date
2026-04-28
Exact day · Estimated
147d ago
As stated: “2026-04-28
Research probability
This event is not joined to a researched indication.
Runway vs event
Cash or burn is missing, so no runway verdict is made.
Model value at stake
Research for this company needs an account. The sample companies are fully interactive without one.

Resolved

Success on 2026-09-21, state resolved.

Sources and detail

Float
No public float has been reported at a usable date.
Stake
Research for this company needs an account. The sample companies are fully interactive without one.
Runway vs event
Cash or burn is missing, so no runway verdict is made.
Financing
No financing filing in the period covered.
Specialist holders
No specialist 13F quarter has been read for this issuer.
Insider net 90d
No open-market insider transaction was filed in the window.

What happened

Success · 2026-09-21.

This event resolved, on the document and quote below.

Sources (2)

  • ClinicalTrials.gov · NCT05535946

    clinicaltrials gov · published 2026-07-07 · retrieved 2026-09-21

    primaryCompletionDateStruct: {"date": "2026-04-28", "type": null}
  • SEC EDGAR

    sec filing · published 2026-09-21 · retrieved 2026-09-22

    On June 1, 2026 , we announced positive results from Part 1 of the Phase 3 ABTECT 44-week maintenance trial, demonstrating strong efficacy, including robust endoscopic remission, and on June 29, 2026, we announced positive topline results from Part 2 of the maintenance trial.

Research

This event is not joined to a researched indication.

Research date unknown

Market

Market linking is switched off.

Quotes elsewhere

This desk holds no price. These go to the venues that publish one.

What counts as each outcome

Resolved by the sponsor's topline disclosure of the trial's primary endpoint: met with statistical significance is success; missed is failure; co-primary endpoints split, or significance reached only in a pre-specified subgroup, is mixed.

Missing inputs

  • issuer_facts: not collected
  • public_float_usd: not collected
  • shares_outstanding: not collected
  • cash_and_investments: not collected
  • operating_cash_flow: not collected
  • quarterly_burn: not collected
  • runway_quarters: not collected

Event row last changed 2026-09-22 · filing signals evaluated 2026-09-22

What changed on this event

  1. · created · event · — → Primary completion of ABTECT - Maintenance · clinicaltrials_gov-candidate
  2. · status · review_state · pending → published · government-source
  3. · date passed · resolution_state · not_watched → date_passed · Guided window closed 86 days ago with no announcement.
  4. · resolved · status · upcoming → resolved · verified against the primary 6-K (2026-06-02, accession 0001193125-26-252360): obefazimod met the FDA primary endpoint of placebo-adjusted clinical remission at Week 44 in both the 25mg (p<0.0001) and 50mg (p<0.0001) arms of ABTECT Part 1; June 29 6-K (Part 2) reports exploratory non-responder/relapser data only, not the primary readout; resolving success on the Part 1 primary-endpoint result
  5. · resolved · outcome · — → success · verified against the primary 6-K (2026-06-02, accession 0001193125-26-252360): obefazimod met the FDA primary endpoint of placebo-adjusted clinical remission at Week 44 in both the 25mg (p<0.0001) and 50mg (p<0.0001) arms of ABTECT Part 1; June 29 6-K (Part 2) reports exploratory non-responder/relapser data only, not the primary readout; resolving success on the Part 1 primary-endpoint result
  6. · resolved · resolved_at · — → 2026-09-21 · verified against the primary 6-K (2026-06-02, accession 0001193125-26-252360): obefazimod met the FDA primary endpoint of placebo-adjusted clinical remission at Week 44 in both the 25mg (p<0.0001) and 50mg (p<0.0001) arms of ABTECT Part 1; June 29 6-K (Part 2) reports exploratory non-responder/relapser data only, not the primary readout; resolving success on the Part 1 primary-endpoint result
  7. · resolved · resolution_state · date_passed → resolved · verified against the primary 6-K (2026-06-02, accession 0001193125-26-252360): obefazimod met the FDA primary endpoint of placebo-adjusted clinical remission at Week 44 in both the 25mg (p<0.0001) and 50mg (p<0.0001) arms of ABTECT Part 1; June 29 6-K (Part 2) reports exploratory non-responder/relapser data only, not the primary readout; resolving success on the Part 1 primary-endpoint result

This is a dated event and its evidence, not a forecast of its outcome. No price, implied move or market probability is collected or shown anywhere on this page.

What was expected, what happened and what changed

Share this event

$AAVXF Phase 3 topline — 28 Apr 2026 (estimated). The date, its source and every figure behind it: https://getfuzebio.com/catalysts/aavxf-abx464-phase3-topline-867ab432?utm_source=x&utm_medium=social&utm_campaign=event&utm_content=event-ev_867ab4327cce2b81

The card this link unfurls to — it carries the date, its confidence and the figures above, and nothing that is not on this page.

Canonical link: https://getfuzebio.com/catalysts/aavxf-abx464-phase3-topline-867ab432

Composed 2026-09-22 · event table maintained 2026-09-22. Assembling this page is not evidence that the sources under it were re-read.