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Q32 Bio QTTB · USD

Health Care · US listing · 🇺🇸 United States

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9.34

+0.97%

Close of 9 Nov 2026, in USD

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About Q32 Bio

From its filings with the US Securities and Exchange Commission

SEC filings

Q32 Bio is based in Waltham, Massachusetts and is incorporated in Delaware. Its shares trade on Nasdaq under the ticker QTTB. The SEC classifies its business as pharmaceutical preparations. In the fiscal year to 31 December 2025, it reported revenue of $53.7m and net income of $29.8m. At that date it held total assets of $61.8m and shareholders' equity of $42.0m.

In its own words

We are a clinical stage biotechnology company focused on developing novel biologics to effectively and safely restore healthy immune balance in patients with alopecia areata (“AA”) and other autoimmune and inflammatory diseases driven by pathological immune dysfunction.

Bempikibart (ADX-914), our most advanced product candidate, is a fully human anti–interleukin-7 receptor alpha (“IL-7Rα”), antagonist monoclonal antibody designed to re-regulate adaptive immune function by potently blocking signaling mediated by interleukin-7 (“IL-7”), and thymic stromal lymphopoietin (“TSLP”). We have completed two Phase 2a clinical trials evaluating bempikibart, SIGNAL-AA Part A, for the treatment of AA, and SIGNAL-AD, for the treatment of atopic dermatitis (“AD”).

In December 2024, we announced topline results from both of these trials, as well as our intention to advance bempikibart for the treatment of AA. In April 2025, we announced dosing of the first patients in both the Part A open-label extension and Part B of the SIGNAL-AA Phase 2a clinical trial and in October 2025, we announced completion of enrollment in SIGNAL-AA Part B. Bempikibart is being evaluated for the treatment of AA in the ongoing Part B of the SIGNAL-AA Phase 2a clinical trial. Enrollment has been completed in the Part B portion of the clinical trial, with 33 patients enrolled, and dosing remains ongoing. We expect to report 36-week topline data from the SIGNAL-AA Part B trial in mid-2026.

Quoted from its 10-K, filed 10 Mar 2026. Read the filing on SEC.gov ↗

Company facts

Sector
Health Care
Industry
Biotechnology
Listed since
28 Mar 2018
Employees
24
Head office
830 WINTER STREET, WALTHAM, MA, 02451
Incorporated in
DE
Classification
Pharmaceutical Preparations
Filer status
Non-accelerated filer<br>Smaller reporting company

Leadership

Pay as last reported

  • Mr. Mark IwickiIndependent Chairman of the Board$414,531
  • Mr. Lee KalowskiPresident, Chief Financial Officer$2.9m
  • Ms. Jodie MorrisonChief Executive Officer, Director, since 2024$6.0m
  • Dr. Shelia VioletteChief Scientific Officer, President of Research$716,221
  • Dr. Jason CampagnaChief Medical Officer$1.5m
  • Dr. Adrien SiposInterim Chief Medical Officer
  • Dr. Arthur TzianabosDirector$216,034
  • Dr. David GrayzelIndependent Director$199,099
  • Ms. Kathleen LaporteIndependent Director$223,662
  • Dr. Bill LundbergIndependent Director$217,530
  • Dr. Isaac MankeIndependent Director$199,865
  • Ms. Mary ThistleIndependent Director$222,631

Environmental, social and governance

Scores out of 100, from our data supplier

ESG
Overall
59
Environment
61
Social
77
Governance
38
Carbon reduction policy
No
Human rights policy
No

SWOT analysis

AI-generated by our data supplier. Not written or checked by our editors.

AI-generated

Strengths

  • HMI-102 is a gene therapy for the treatment of phenylketonuria.
  • The company employs 205 full-time employees in the biotechnology sector.
  • 15 adeno-associated virus vectors enable precise gene correction methods.

Weaknesses

  • The company has only 24 employees listed in the data.
  • Bedford is the headquarters city for Homology Medicines, Inc.
  • The listing date was 28 March 2018 on the market.

Opportunities

  • The pipeline targets rare diseases at the genetic level globally.
  • Gene therapy approaches focus on adults with monogenic diseases.
  • Single intravenous injections target liver, CNS, and other tissues.

Threats

  • Monogenic diseases in the liver require complex genetic treatments.
  • Central nervous system treatments face significant biological delivery challenges.
  • Bone marrow and lung therapies involve high development risks.

Sources and methodology

Data on this tab
Our data supplier
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