BMEA · Biomea Fusion
Conviction · Low · more likely to lag the S&P 500 over the next three months
Wrong if: a daily close above $0.73
Note written ·
Price against the kill line
20.2% clear of its kill line on the 13 November 2026 close.
How to read this
This note expects the shares to lag the market, so its kill line sits above the price: a close above the red mark would prove the view wrong. Prices run from low on the left to high on the right. The dot is where the stock closed on 13 November 2026, left of the mark while it is below the line; a dot right of the mark has closed through it.
The scale is stretched near the line, so close calls are easy to see. More than 8% from the line, the stock reads well clear, with a hollow dot to show the figure is off the drawn scale.
The kill line is the research note's own test. The portfolio sells on business facts, not on a price. How the portfolio decides
Three months against the kill line
Daily closes, to . Red: the kill line, a daily close above $0.7300, on record since 11 November 2026. The shares are down 56.9% since the close; the S&P 500 is down 2.1% over the same sessions. Figures in the note can cover a different window.
Kill line
A daily close above $0.73, about 30% over the last close, would show the shares leading the S&P 500. So would a signed BMF-650 partnership or licence with an upfront payment.
Research onlyNot in the portfolio.
Catalyst
Key figures from the filings · Health Care
Quarter to 30 September 2026, filed 10 November 2026
- Net cash, cash less debt ($M)
- 26.4
All filed numbers
What Biomea Fusion reports to the SEC in its quarterly and annual filings. Each group states its period and filing date once; a figure dated otherwise says so. Built from the filings known on .
| Pre-tax income ($M) | Not reported |
| Net income ($M) four quarters: −22.3 | −6.2 |
| Diluted shares, change on a year (%) against the quarter to 30 September 2025 | +21.3 |
| Operating cash flow ($M) | −44.1 |
| Capital spending ($M) four quarters to 30 September 2025, filed 24 March 2026 | 0.1 |
| Free cash flow ($M) | Not available |
| Cash and short-term investments ($M) | 26.4 |
| Debt ($M) | None reported |
| Net cash, cash less debt ($M) no debt reported | 26.4 |
| Deferred revenue ($M) | Not reported |
| Backlog, orders not yet delivered ($M) | Not reported |
| Receivables ($M) | Not reported |
| Inventory ($M) | Not reported |
| Shareholders' equity ($M) | 7.6 |
| Market value ($M) | 42.3 |
| Enterprise value, market value plus net debt ($M) no debt reported | 15.9 |
| Enterprise value to sales (×) | Not available |
| Enterprise value to operating income (×) | Not meaningful |
| Price to earnings (×) | Not meaningful |
| Price to book value (×) | 5.6 |
| Free-cash-flow yield (%) | Not available |
Short interest (FINRA, settled 15 October 2026, published 26 October 2026): 21.6% of shares outstanding sold short, 4.8 days of average trading to cover, +11.6% since the previous report.
| Window | Bought | Sold |
|---|---|---|
| 90 daysfrom | $0 | $0 |
| 12 monthsfrom | $196K | $0 |
The thesis
Biomea Fusion is more likely to lag the S&P 500 over the next three months. Its cash fell to $26.8 million at 30 September 2026 from $35.2 million at 30 June 2026, the oral GLP-1 drug BMF-650 has no partner, and the company has not completed a financing since withdrawing its September offering. The shares closed at $0.56 on 12 November 2026, and the 16 November 2026 ObesityWeek poster and any financing or partnership news settle whether that view holds.
The third-quarter report arrived on 10 November 2026, when the company also filed its Form 10-Q. Net loss was $6.2 million against $16.4 million a year earlier, research and development spending was $8.5 million against $14.4 million, and general and administrative spending was $4.4 million (BiopharmaWatch summary of the release). Biomea still projects cash into the second quarter of 2027, the same runway it gave in August. The Q2 2026 Form 10-Q carried substantial-doubt going-concern language.
The shares did not rally on the report. They closed at $0.55 on 10 November 2026, $0.61 on 11 November 2026 and $0.56 on 12 November 2026.
Bullish and bearish views on Biomea Fusion, Inc.
The bull case on Biomea Fusion, Inc. (BMEA), in brief: weight loss appeared in every cohort. The bear case: cash is short and falling.
Bull case
- Weight loss appeared in every cohort. In outpatient cohorts 1–4, mean weight reduction at Day 29 ranged from 1.5% to 3.2%, against 0.1% for pooled placebo (company press release, 13 October 2026).
- The highest-dose group lost 6.1%. The confined fifth cohort lost a mean 6.1% (6.2 kg) by Day 29 on 200 mg daily for one week, then 400 mg daily for three weeks (company press release, 13 October 2026).
- Tolerability looked clean. Biomea reported no severe or serious treatment-emergent adverse events among 40 BMF-650-treated participants. Nausea was 17.5% and vomiting 7.5% (press release summarised by AllSci, 14 October 2026).
- Spending is falling. Research and development cost was $8.5 million in the third quarter of 2026, against $14.4 million a year earlier, and the quarterly loss narrowed to $6.2 million from $16.4 million (BiopharmaWatch summary of the 10 November 2026 release). Biomea reported a third-quarter loss of $0.09 per share against a $0.21 estimate (company news, 10 November 2026).
- A partner would change the funding picture. Biomea said on 10 November 2026 that it will pursue a strategic partnership, including licensing for late-stage development and commercialisation of BMF-650. It will present the Phase I results at ObesityWeek on 16 November 2026.
Bear case
- Cash is short and falling. Cash, equivalents and restricted cash were $26.8 million at 30 September 2026, against $56.2 million at 31 December 2025 and $35.2 million at 30 June 2026 (BiopharmaWatch summary of the 10 November 2026 release; Q2 2026 Form 10-Q). Runway is guided only into the second quarter of 2027.
- The going-concern warning stands. The Q2 2026 Form 10-Q states that resources will not fund operations for twelve months past issuance. The accumulated deficit was $469.8 million at 30 June 2026.
- A financing was attempted and withdrawn. Biomea announced a public offering on 22 September 2026 and terminated it on 23 September 2026, citing market conditions; no securities were sold (Benzinga, 23 September 2026). An effective Form S-3 shelf registration allows new shares to be issued quickly.
- The placebo comparison is muddied. The two placebo participants in the confined cohort also lost weight, and Biomea said this complicates placebo-adjusted interpretation (company press release, 13 October 2026).
- BMF-650 needs more work and outside money. Biomea says further development requires longer-term toxicology studies, and it plans 13-week toxicology work before Phase II weight-loss trials (MarketBeat, 13 October 2026). No partner has been announced.
- Selling has continued after the data. The close fell from $0.83 on 14 October 2026 to $0.56 on 12 November 2026, and the shares fell 57.4% over three months (adjusted daily closes).
Price setup
The shares closed at $0.56 on 12 November 2026. That is 75.0% below the 52-week intraday high of $2.24 on 20 April 2026. The 52-week closing low is $0.55, set on 10 November 2026, two sessions earlier. The 3-month reference close was $1.32 on 14 August 2026.
The 50-day average is $1.16 and the 200-day average is $1.34, both as of the 12 November 2026 close. The shares trade well under both, and under $1.00 in every session from 5 November to 12 November 2026. Nasdaq's minimum-bid rule is breached after 30 consecutive business days of closes below $1.00, and the company would disclose a notice on Form 8-K.
The price already reflects a high chance of dilution: at $0.56 the shares trade 75.0% under their April high, with $26.8 million of cash at 30 September 2026 and no partner or completed financing announced.
Catalysts ahead
- 16 November 2026: ObesityWeek 2026 poster presenting the BMF-650 Phase I results (poster 828, National Harbor, Maryland), announced by the company on 10 November 2026. It adds detail on dose response, placebo comparison and tolerability that a prospective licensing partner would weigh.
- ~31 March 2027 (est.): COVALENT-211 topline on the 26-week HbA1c primary endpoint, guided for the first quarter of 2027. This placebo-controlled result tests icovamenib's glucose-control claim, and it falls after the guided runway of the second quarter of 2027 begins to tighten.
What would change the view
A daily close above $0.73, about 30% over the last close, would show the shares leading the S&P 500. So would a signed BMF-650 partnership or licence with an upfront payment.
What it trades with
BMEA trades on its own financing, partnership and trial news. Sentiment in the oral GLP-1 field sets the backdrop for any licensing talks over BMF-650, and risk appetite for small-cap biotech funding rounds affects whether a new offering can price.
The evidence, claim by claim (8)
- Cash, equivalents and restricted cash were $26.8 million at 30 September 2026, against $56.2 million at 31 December 2025; runway is projected into the second quarter of 2027. Third quarter 2026 results release (via BiopharmaWatch summary) · as of
- Third-quarter 2026 net loss was $6.2 million against $16.4 million a year earlier; research and development was $8.5 million against $14.4 million; general and administrative was $4.4 million. Third quarter 2026 results release (via BiopharmaWatch summary) · as of
- Biomea reported a third-quarter loss of $0.09 per share against a $0.21 estimate. Company news headline · as of
- BMF-650 Phase I: outpatient cohorts 1–4 showed mean Day 29 weight reduction of 1.5% to 3.2% versus 0.1% for pooled placebo; confined cohort 5 lost a mean 6.1% (6.2 kg), and its two placebo participants also lost weight. Biomea Fusion press release · as of
- No severe or serious treatment-emergent adverse events among 40 BMF-650-treated participants; nausea 17.5%, vomiting 7.5%. Biomea Fusion press release via AllSci · as of
- Biomea terminated its proposed public offering on 23 September 2026, citing market conditions; no securities were sold. Biomea Fusion press release via Benzinga · as of
- Cash, equivalents and restricted cash were $35.2 million at 30 June 2026; the 10-Q states substantial doubt about continuing as a going concern. Second quarter 2026 Form 10-Q and results release · as of
- COVALENT-211 enrolment is complete; topline on the 26-week primary endpoint (HbA1c reduction) is guided for the first quarter of 2027. Third quarter 2026 results release (via BiopharmaWatch summary) · as of
Sources
Related · shared themes
VKTX
Viking Therapeutics
Viking Therapeutics is more likely to lag the S&P 500 over three months: $960 million in cash funds its obesity Phase 3 trials, but no…
VERU
Veru
Veru's case rests on whether its oral drug enobosarm preserves lean mass alongside semaglutide; the PLATEAU 32-week interim, guided to…
LLY
Eli Lilly
Eli Lilly's shares are more likely than not to beat the S&P 500 over three months, as tirzepatide volume still outruns price cuts and…
AMGN
Amgen
Amgen is modestly more likely than not to beat the S&P 500 over three months because Repatha, Evenity and newer drugs are outgrowing…