Q32 Bio Inc. (QTTB) Stock Price & How to Invest
Last updated July 2026
Short answer
QTTB is Q32 Bio Inc., a 24-person clinical-stage biotech in Waltham, Massachusetts whose entire equity story is bempikibart, an anti-IL-7R alpha antibody being developed for severe alopecia areata. Anyone buying QTTB is buying one unpartnered Phase 2a asset that produced positive open-label Week 36 data in July 2026, plus roughly $294 million of cash raised on the back of it, and nothing that generates product revenue.
QTTB stock price
As of 2026-08-21, Q32 Bio Inc. (QTTB) last closed at $15.97, up 736.1% over the past year. Over the past 52 weeks it has traded between $1.66 and $21.38.
Prices are daily closing prices from Yahoo Finance and may be delayed. For the live quote, check your broker or Q32 Bio Inc.'s investor relations page. Walnut is informational, not investment advice.
What does Q32 Bio Inc. (QTTB) do?
Q32 Bio Inc. is a clinical-stage biotechnology company focused on alopecia areata (AA) and other autoimmune and inflammatory diseases. Its lead and effectively only clinical program is bempikibart (ADX-914), a fully human monoclonal antibody that blocks the interleukin-7 receptor alpha chain and therefore shuts down signaling from both IL-7 and TSLP, two pathways implicated in the T-cell attack on hair follicles. The company reached the public market by reverse-merging into Homology Medicines in March 2024, which is why the CIK on EDGAR still carries the old FIXX ticker, and it trades on the Nasdaq Capital Market with about 24 employees under CEO Jodie Morrison. Its history since then has been a sequence of narrowing decisions: bempikibart missed in atopic dermatitis (the SIGNAL-AD trial, topline December 2024), the company restructured in February 2025 to focus on AA, and in November 2025 it sold the entire ADX-097 complement program to Akebia Therapeutics. What remains is bempikibart, a preclinical half-life-extended follow-on called ADX-914-XL, and a retained tissue-targeted complement platform (ADX-096 and related molecules) that management describes as under strategic review.
The investment picture turns on two facts that arrived in July 2026. First, Q32 reported 36-week topline results from SIGNAL-AA Part B, an open-label trial in 33 patients with severe or very severe AA: a mean SALT score reduction of ~35.3% in the modified intent-to-treat population, with ~40.0% (10 of 25) achieving a SALT20 response in the mITT analysis and ~30.3% (10 of 33) in the full intent-to-treat set. Second, the company sold ~6.03 million shares at $18.25 plus pre-funded warrants for another ~4.93 million shares, taking in ~$187.6 million net. Added to the ~$106.3 million on hand at June 30, that is roughly ~$294 million against a market value near ~$473 million at ~$15.90 per share, and the company states the money is sufficient to reach topline Phase 3 results of the registration-directed program it intends to start in the first half of 2027. The reported ~$53.7 million of trailing revenue and the resulting single-digit trailing P/E are accounting artifacts, not a business: they come from derecognizing a ~$55.0 million refund liability owed to Amgen in the fourth quarter of 2025. Q32 has never recorded a dollar of product revenue and does not expect to for years.
What's driving Q32 Bio Inc. (QTTB)?
1. Bempikibart and the path to a registration-directed program
SIGNAL-AA Part B enrolled 33 patients with baseline SALT scores of 50 to 100, dosed 200mg weekly for four loading doses and then every other week through Week 36, with ~36.4% having prior exposure to oral JAK inhibitors. At Week 36 the mITT analysis showed a ~35.3% mean reduction in SALT score, with ~44.0% (11 of 25) reaching SALT30 and SALT50 responses, and the off-drug follow-up through Week 52 is still running with signs of maintained or deepening response. Management plans regulatory discussions later in 2026 and intends to move into a registration-directed program in the first half of 2027, with completed open-label-extension results expected in the second half of 2027.
2. A balance sheet that now outlasts the next trial
At June 30, 2026 Q32 held ~$106.3 million of cash against ~$10.0 million of total liabilities, having paid off the remaining ~$6.8 million of Silicon Valley Bank venture debt on June 24 and left itself debt-free. The July 2026 follow-on added ~$187.6 million net, and a 30-day underwriters' option for up to ~1,643,835 further shares was granted on top of that. Cash burn has been modest while the company waited on data, at ~$9.4 million of net cash used in operations across the first half of 2026 versus ~$23.1 million in the same period of 2025, though Phase 3 spending will change that shape quickly.
3. Value sitting outside the lead trial
The ADX-097 sale to Akebia Therapeutics in November 2025 brought ~$7.0 million upfront and ~$3.0 million at the six-month mark, with a further ~$2.0 million due on the earlier of a first milestone or December 31, 2026, and leaves Q32 eligible for up to ~$580 million of milestones (~$92.5 million development and regulatory, ~$487.5 million commercial) plus tiered royalties from low single digits to mid-teens on any future sales. Separately, the November 7, 2025 Amgen Amendment retired every remaining regulatory and sales milestone owed on bempikibart for a one-time grant of ~553,695 shares, which is why Q32 now owns the asset outright. The retained complement platform (ADX-096 and related C3d fusions and nanobodies) carries no assigned value in the current price and is described as under strategic evaluation.
4. A mechanism that is not another JAK inhibitor
The three approved treatments for severe alopecia areata are all oral JAK inhibitors: Eli Lilly's Olumiant (baricitinib), Pfizer's Litfulo (ritlecitinib) and Sun Pharma's Leqselvi (deuruxolitinib), each of which carries class boxed warnings covering serious infection, mortality, malignancy, major cardiovascular events and thrombosis. Bempikibart is a subcutaneous antibody with a different mechanism and, across more than 150 participants dosed to date, no treatment-related Grade 3 or higher adverse events, with injection site reactions (reported in ~36.3% of Part B patients but only ~4% of doses) as the most common finding. Whether a differentiated safety profile is worth a lower response rate than the JAK inhibitors is the commercial question the Phase 3 program exists to answer.
What are the risks to Q32 Bio Inc. (QTTB)?
The concentration risk is total: one unpartnered asset, one indication, and a company that already watched bempikibart fail to earn a path forward in atopic dermatitis before it restructured around AA in February 2025. The July data came from an open-label single-arm trial of 33 patients with no placebo control, and the headline numbers rest on a 25-patient mITT population, so eight of the 33 enrolled patients sit outside the primary analysis and the ITT figures are materially lower (~30.3% versus ~40.0% on SALT20); alopecia areata trials have a long history of placebo responses and spontaneous regrowth that a single-arm design cannot separate out. The economics of a future partnership are encumbered, because bempikibart is in-licensed from Bristol-Myers Squibb under a 2019 agreement that entitles BMS to development and regulatory milestones of ~$32 million to ~$49 million per indication for the first three indications, up to ~$215 million of commercial milestones, royalties from mid-single digits to ~10%, and up to ~60% of any sublicense income, a share that falls only as the program advances. Dilution has been continuous and is not finished: the share count went from ~12.9 million at the end of 2025 to ~29.8 million by August 3, 2026 through a February registered direct, a March ATM with Cantor Fitzgerald, a May private placement at $8.00 and the July follow-on at $18.25, there are ~6.1 million pre-funded warrants outstanding on top of that, and the company states plainly that its cash will not carry any program to regulatory approval. Finally, the listing itself has been fragile before, with a May 19, 2025 Nasdaq notice for falling below the $2.5 million stockholders' equity minimum under Listing Rule 5550(b)(1) that was only cured on the strength of the Q4 2025 accounting gain and subsequent raises, and a stock that ranged from ~$1.62 to ~$23.57 within twelve months is not one where position sizing is a detail.
What is the Q32 Bio Inc. (QTTB) forecast?
4 analysts publish price targets on QTTB, averaging $42.75 against a $15.97 price as of August 2026, or +167.7%. The published targets run from $36.00 to $59.00, a moderate spread, and the ratings split 5 buy, 0 hold, 0 sell. Over the last six months there have been 2 raises and 0 cuts among the published actions. A price target is what an analyst published on a date, not a prediction, and sell-side ratings skew positive across the whole market.
Read the full QTTB forecast and price target for the target table, the recent rating actions by firm, and how the consensus has shifted.
Is QTTB a buy or a sell?
We give no verdict on Q32 Bio Inc.. Both cases are real, which is why the question is contested at all, so here is the strongest version of each.
The case for buying. Bempikibart and the path to a registration-directed program. SIGNAL-AA Part B enrolled 33 patients with baseline SALT scores of 50 to 100, dosed 200mg weekly for four loading doses and then every other week through Week 36, with ~36.4% having prior exposure to oral JAK inhibitors. The most optimistic published target, $59.00, assumes this works close to its best case.
The case against. The concentration risk is total: one unpartnered asset, one indication, and a company that already watched bempikibart fail to earn a path forward in atopic dermatitis before it restructured around AA in February 2025. The most pessimistic target, $36.00, is roughly what QTTB is worth if this bites instead.
Read the full bull and bear case on QTTB, including what would have to change to break either one. Walnut is not an investment adviser.
How is Q32 Bio Inc. (QTTB) valued? (approximate, August 2026)
A simple financial snapshot. These are approximations and refresh quarterly; for current figures see Q32 Bio Inc.'s investor relations page or your broker.
- Revenue (TTM): ~$53.7 million, all of it recognized in the fourth quarter of 2025 and none of it product revenue: it is the derecognition of a ~$55.0 million refund liability from the terminated Horizon collaboration, settled with Amgen on November 7, 2025 for ~553,695 shares. Revenue in the first half of 2026 was ~$0
- Loss rate: Net loss of ~$8.9 million in Q2 2026 and ~$16.6 million for the first half, on operating expenses of ~$16.8 million (R&D ~$7.5 million, G&A ~$9.4 million); net cash used in operations was ~$9.4 million for the half versus ~$23.1 million a year earlier. Accumulated deficit stands at ~$221.5 million
- Cash and runway: ~$106.3 million of cash and equivalents at June 30, 2026, plus ~$187.6 million net from the July 16 follow-on, for roughly ~$294 million before third-quarter spending. Management states this funds operations through topline Phase 3 results of the planned registration-directed program, and explicitly not through regulatory approval
- Balance sheet: Total assets ~$115.9 million against total liabilities ~$10.0 million and stockholders' equity ~$105.9 million at June 30, 2026, all before the July raise. Debt-free since the ~$6.8 million Silicon Valley Bank venture-debt payoff on June 24, 2026
- Program spend: Direct R&D on bempikibart was ~$2.4 million in Q2 2026 and ~$3.7 million for the half; ADX-097 spending fell to ~$0 after the Akebia sale, from ~$1.5 million in the first half of 2025. The company employs ~24 people
- Market pricing: ~$15.90 per share for a market value near ~$473 million on ~29,769,466 shares outstanding as of August 3, 2026, with ~21.0 million of public float and ~6.1 million pre-funded warrants outstanding on top. Counting those warrants, equity value is closer to ~$570 million and enterprise value near ~$276 million. 52-week range ~$1.62 (September 4, 2025) to ~$23.57 (July 14, 2026)
Figures are approximate, tied to August 2026 and drawn from the Q2 2026 10-Q filed August 5, 2026 and the fiscal 2025 10-K, so check live data before acting on any of them. Two screen-level numbers on QTTB are misleading and worth discarding: the ~5.3x trailing P/E and the ~8.8x price-to-sales both derive from the ~$53.7 million of one-time non-cash collaboration revenue and the ~$29.8 million of 2025 net income it produced, and neither describes an operating business. The number that carries information is enterprise value, roughly ~$276 million once the ~$294 million of pro forma cash is netted against the fully-funded equity value, which is what the market is assigning to bempikibart, the retained complement platform and the Akebia royalty stream combined.
Who competes with Q32 Bio Inc. (QTTB)?
Approved alopecia areata treatments
Three oral JAK inhibitors hold the severe-AA market: Eli Lilly's Olumiant (baricitinib), Pfizer's Litfulo (ritlecitinib) and Sun Pharma's Leqselvi (deuruxolitinib). They set both the efficacy bar bempikibart has to clear and the safety opening it is aiming at, since the class carries boxed warnings for serious infection, mortality, malignancy, major cardiovascular events and thrombosis. Any Phase 3 readout from Q32 will be judged against SALT response rates already established by drugs a dermatologist can prescribe today.
Immunology developers targeting the same pathways
IL-7R alpha and TSLP are crowded targets across immunology. Bristol Myers Squibb originated the bempikibart antibody and retains license economics on it, OSE Immunotherapeutics is developing the anti-IL-7R antibody lusvertikimab, and AstraZeneca and Amgen market Tezspire (tezepelumab) against TSLP in asthma, which means large-cap programs are validating and competing for the same biology from adjacent indications. Q32 competes with these companies for clinical investigators, manufacturing slots and, if it ever seeks a partner, for attention.
Other single-asset autoimmune microcaps
For an investor, QTTB's closest comparables are not the large pharmas but other small clinical-stage immunology names whose value moves on single readouts, where the shared characteristics are no revenue, repeated equity raises and a share price that can move by multiples on one press release. Q32's own 52-week path from ~$1.62 to ~$23.57 and back to ~$15.90 is the pattern. The distinguishing feature within that group is the balance sheet: roughly ~$294 million pro forma against a ~$473 million market value is unusually well capitalized for the cohort.
What stocks are similar to Q32 Bio Inc. (QTTB)?
Other names that sit close to QTTB: same theme, named as a direct competitor, or held beside it in the same funds. Each entry says which. Worth a look if you are thinking about diversification within a thesis rather than concentration on one ticker.
How to invest in Q32 Bio Inc. (QTTB)
There are three common ways to get QTTB exposure. Buy shares (or fractional shares) directly at any major broker. Hold an ETF that includes it, which spreads the position across many companies. Or build it into a focused thematic portfolio, so QTTB sits alongside other stocks that express the same thesis.
Walnut takes the portfolio route. Describe a thesis where QTTB fits (for example “AI infrastructure” or “dividend-growth large-caps”) and the AI proposes 5 to 6 constituents with target weights. You review the plan and fund it through your own broker when you're ready.
New to this? Start with how to invest in stocks, see how to analyze a stock with AI, or compare the best AI stock analyzers.
The bottom line on Q32 Bio Inc. (QTTB)
Q32 Bio in August 2026 is a single-asset autoimmune bet whose balance sheet finally matches its ambition, priced at roughly $276 million of enterprise value on 33 patients of open-label data and a Phase 3 that has not started.
More on Q32 Bio Inc. (QTTB)
Whether QTTB is worth buying today depends more on your time horizon and what you already hold than on any single call. We walk through valuation, what would have to go right, and the risks in is QTTB a buy or a sell?, and where the stock could go from here in the QTTB stock forecast.
For income investors, whether QTTB pays a dividend and how the payout looks is covered in does QTTB pay a dividend? And to weigh QTTB against a peer, read the full side-by-side comparisons: QTTB vs AA and QTTB vs LLY.
Wondering how QTTB fits the portfolio you already own? Walnut is an AI investing app that connects your brokerage read-only and answers questions like that about your actual holdings: overlap, concentration, and how each position tracks the S&P 500. Compare the best AI portfolio analyzers or see the best AI investing apps in 2026.
Investing in Q32 Bio Inc. with AI
Connect the broker you already use and ask Walnut's AI how QTTB fits what you actually hold: whether you own it already through a fund, what it would do to your concentration, and how it has tracked the S&P 500. Read-only by default, and you approve anything before it reaches your broker.
FAQ
What does Q32 Bio actually do?
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It develops bempikibart (ADX-914), a fully human antibody that blocks the interleukin-7 receptor alpha chain and therefore suppresses signaling from both IL-7 and TSLP, for severe alopecia areata. It has no approved products, no sales force and no product revenue, and employs about 24 people from offices in Waltham, Massachusetts. The remaining pipeline is thin by design: ADX-914-XL, a half-life-extended version of the same antibody, is preclinical, and the tissue-targeted complement platform (ADX-096 and related molecules) is retained but not funded, described in filings as under evaluation for strategic options.
Why does QTTB show ~$53.7 million of revenue and a single-digit P/E if it sells nothing?
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Because of an accounting reversal, not a sale. In 2022 Q32 received ~$55.0 million from Horizon Therapeutics under a collaboration on bempikibart. When that agreement was terminated in November 2023, the money stayed with Q32 but was reclassified as a refund liability owed against future milestone payments. On November 7, 2025 Q32 issued Amgen (which had acquired Horizon) a one-time grant of ~553,695 shares to extinguish every remaining milestone obligation, so the liability was derecognized and the difference was booked as collaboration revenue in the fourth quarter of 2025. That produced ~$53.7 million of revenue and ~$29.8 million of net income for 2025 with no cash changing hands, and it is the sole reason a screen shows QTTB as profitable.
What did the SIGNAL-AA Part B results actually show?
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Q32 reported 36-week topline data in July 2026 from an open-label trial of 33 patients with severe or very severe alopecia areata (baseline SALT scores of 50 to 100), of whom ~36.4% had already been treated with oral JAK inhibitors. In the modified intent-to-treat population the mean SALT score fell ~35.3% from baseline, with ~40.0% (10 of 25) reaching a SALT20 response and ~44.0% (11 of 25) reaching SALT30 and SALT50. Across the full 33-patient intent-to-treat set those figures are ~30.3% and ~33.3%. There was no placebo arm, no serious or Grade 3 or higher treatment-related adverse events were reported, and the off-drug follow-up through Week 52 is still running.
How much cash does Q32 Bio have, and how long does it last?
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The company held ~$106.3 million at June 30, 2026 and raised ~$187.6 million net in the July 16 follow-on offering, for roughly ~$294 million before third-quarter spending, with no debt after paying off the ~$6.8 million Silicon Valley Bank facility on June 24. Management's own statement is that this funds operations through topline Phase 3 results from the planned registration-directed program, and the same filing says explicitly that it will not carry any program to regulatory approval. Recent burn has been light at ~$9.4 million of operating cash use across the first half of 2026, but that reflects a company waiting on data rather than one running a pivotal trial.
Why did QTTB move from about $1.62 to above $23 within a year?
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The low on September 4, 2025 followed a difficult stretch: bempikibart did not earn a path forward in atopic dermatitis, the company restructured in February 2025 around alopecia areata alone, and on May 19, 2025 Nasdaq notified it that stockholders' equity had fallen below the $2.5 million minimum under Listing Rule 5550(b)(1). The recovery came in stages: the Amgen settlement and the Akebia sale in November 2025 repaired the balance sheet and restored listing compliance, financings in February, March and May 2026 added cash, and the July 2026 SIGNAL-AA Part B topline carried the stock to a ~$23.57 high on July 14. It has since traded back toward ~$15.90.
What happened to ADX-097 and the complement platform?
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ADX-097, a humanized anti-C3d antibody fusion protein that had completed Phase 1, was sold to Akebia Therapeutics in November 2025 along with the underlying University of Colorado license. Q32 received ~$7.0 million upfront and ~$3.0 million on the six-month anniversary, is owed a further ~$2.0 million on the earlier of a first milestone or December 31, 2026, and retains eligibility for up to ~$580 million of milestones (~$92.5 million development and regulatory, ~$487.5 million commercial) plus tiered royalties from low single digits to mid-teen percentages of net sales. Q32 kept the broader tissue-targeted complement platform, including ADX-096 for ophthalmology, but is not funding it and lists it as a candidate for strategic options.
Is bempikibart partnered, and what does Bristol Myers Squibb get from it?
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It is unpartnered as a development program, which is why Q32 is funding the Phase 3 itself, but it is not unencumbered. Bempikibart is in-licensed from Bristol-Myers Squibb under a September 2019 agreement (amended in 2021 and 2022) for which Q32 paid ~$8 million upfront plus preferred shares and a ~$4.0 million milestone in July 2024. BMS is entitled to development and regulatory milestones of ~$32 million to ~$49 million per indication for the first three indications, up to ~$215 million in commercial milestones, tiered royalties from mid-single digits to ~10% of net sales, and up to ~60% of any sublicense income, a percentage that decreases as the program advances. That last term is the one that shapes how a future partnership would be valued, because partnering earlier hands BMS a larger share.
What are the main things that decide QTTB from here?
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Four things, in rough order of weight. First, whether the regulatory discussions planned for late 2026 produce a registration-directed design the FDA accepts, and whether that program starts in the first half of 2027 as intended. Second, whether the Week 52 off-drug follow-up and the open-label-extension results due in the second half of 2027 hold up the durability signal, since open-label single-arm data in alopecia areata has to survive a controlled trial before it means much. Third, capital: the current cash reaches Phase 3 topline and no further, and the share count has already grown from ~12.9 million to ~29.8 million in eight months with ~6.1 million pre-funded warrants outstanding. Fourth, competitive positioning against three approved oral JAK inhibitors that already treat this disease.
Walnut is informational, not investment advice. Financial figures on this page are approximations; always verify current numbers with Q32 Bio Inc.'s investor relations page or your broker before making investment decisions.