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QTTB US Equity

Q32 Bio Inc.Health Care · Pharmaceutical Preparations · CIK 1661998 · FY ends Dec 31
$15.84
+0.55 (+3.60%)
USD · as of 2026-08-19 · marketstack
3 registered studies · 2 active

Studies where QTTB is the lead sponsor, as filed with ClinicalTrials.gov. Completion dates are the sponsor's own projected windows and are revised as a study runs. Active studies first, then completed and stopped — newest readout first within each.

3 interventional

Held by 10 tracked-famous managers (Point72 Asset Management, L.P., RENAISSANCE TECHNOLOGIES LLC, JANE STREET GROUP, LLC, CITADEL ADVISORS LLC, MARSHALL WACE, LLP, +5 more) · FINRA short interest 3.8 days to cover (settled 2026-07-31) · insider 90d: 4 buys / 0 sells · government filings 180d: none disclosed

StudyPhaseStatusInterventionsConditionsEnrollmentPrimary completionUpdated
A Phase 2a Proof-of-Concept Trial of Bempikibart (ADX-914) for the Treatment of Severe Alopecia Areata (SIGNAL-AA)NCT06018428Part A: Mean relative percent change in SALT scoreOpen-label · TreatmentPhase 2Active, not recruitingDrug: bempikibart (ADX-914)Alopecia Areata75Jun 20262026-05-08
Evaluating Safety and Efficacy of ADX-914 in Patients With Moderate to Severe Atopic Dermatitis (SIGNAL-AD)NCT05509023Part A only: Safety parameters including incidence of serious adverse events and adverse events of special interestRandomized · Triple-masked · TreatmentPhase 2Active, not recruitingDrug: ADX-914, PlaceboAtopic Dermatitis102Dec 20242024-10-03
Single and Multiple Ascending Dose Study of ADX-914 in Healthy Adult VolunteersNCT04485481Number of subjects with adverse eventsRandomized · Quadruple-masked · OtherPhase 1CompletedDrug: ADX-914, Placebo, ADX-914, PlaceboSafety Issues422022-01-12actual2022-07-28

Primary completion is the date the sponsor filed with the registry — their own projection, revised whenever they revise it, unless the row is marked actual.

Source: ClinicalTrials.gov, retrieved 2026-08-19