Altimmune, Inc. (ALT) SEC Filings & Earnings Calls
EquiReason read 18 Altimmune, Inc. SEC filings in the last 12 months. Latest: 8-K on 2026-09-29 — Appointment of Richard Menziuso as VP, Global Controller and Principal Accounting Officer, effective September 29, 2026. Routine executive hire with no material financial impact..
Source: SEC EDGAR filings · figures as of 2026-06-30 · read by EquiReason
- Market cap
- 412.4M
- P/E TTM
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- Dividend yield
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- Next earnings
- 10 Nov, in 17 days
Every filing, read
last 12 months · SECWhat happened, the numbers inside, guidance and risks. The original is one click away.
12 Aug 20268-K · 2.02Cash, cash equivalents and investments $519M; Net loss $-23M (+3% y/y); R&D expenses $19M (+9% y/y)earningsopen
Figures in the filing · each found in the filing text
| Cash, cash equivalents and investments · Q2-2026 | $519M | |
| Net loss · Q2-2026 | $-23M | +3% y/y |
| R&D expenses · Q2-2026 | $19M | +9% y/y |
| G&A expenses · Q2-2026 | $8M | +33% y/y |
| Interest income · Q2-2026 | $5M |
Risks flagged
Increasing net loss and R&D spend without revenue
“Net loss increased to $22.8M from $22.1M; R&D expenses up 8.7%”
12 Aug 202610-QPositive topline results from RECLAIM Phase 2 trial in AUD; Phase 3 MASH trial enrollment started.open
Figures in the filing · each found in the filing text
| Net loss · Q2-2026 | $-23M | |
| Research and development expenses · Q2-2026 | $19M | +8% y/y |
| General and administrative expenses · Q2-2026 | $8M | +33% y/y |
| Interest income · Q2-2026 | $5M | +300% y/y |
| Cash, cash equivalents, restricted cash and short-term investments · 2026-06-30 | $326M | |
| Accumulated deficit · 2026-06-30 | $-695M |
Risks flagged
Clinical trial failure risk
“We have not generated any revenues from the sale of any products to date and there is no assurance of any future revenues from product sales.” · word for word
Dilution risk from warrants
“If all of the common stock warrants sold in the April 2026 Offering were to be exercised in cash at their exercise price, we would receive additional gross proceeds of $225 million.” · word for word
28 Jul 20268-K · 7.01, 8.01Change from baseline in HDD/Week at Week 24 (LS mean) - Pemvidutide -4.2; Change from baseline in HDD/Week at Week 24 (LS mean) - Placebo -2.75; Treatment Effect (LS mean difference) - HDD/Week -1.45open
Figures in the filing · each found in the filing text
| Change from baseline in HDD/Week at Week 24 (LS mean) - Pemvidutide · pemvidutide 2.4 mg · Week 24 | -4.2 | |
| Change from baseline in HDD/Week at Week 24 (LS mean) - Placebo · placebo · Week 24 | -2.75 | |
| Treatment Effect (LS mean difference) - HDD/Week · pemvidutide vs placebo · Week 24 | -1.45 | |
| P-value for primary endpoint · Week 24 | $0.00 | |
| 2-level Reduction in WHO-RDL - Pemvidutide · pemvidutide 2.4 mg · Week 24 | 64.4% | |
| 2-level Reduction in WHO-RDL - Placebo · placebo · Week 24 | 34.8% | |
| Zero HDD in Week 21-24 - Pemvidutide · pemvidutide 2.4 mg · Week 21-24 | 42.2% | |
| Zero HDD in Week 21-24 - Placebo · placebo · Week 21-24 | 17.4% | |
| Change from baseline in Percent of Days with Abstinence (LS mean) - Pemvidutide · pemvidutide 2.4 mg · Week 24 | 38.9% | |
| Change from baseline in Percent of Days with Abstinence (LS mean) - Placebo · placebo · Week 24 | 20.5% |
Risks flagged
Clinical trial risk: Phase 2 results may not replicate in Phase 3; FDA meeting outcome uncertain.
“The Company plans to request an End-of-Phase 2 meeting with the FDA based on the results of the trial.” · word for word
No revenue or profitability; company is pre-commercial.
“Altimmune is a late clinical-stage biopharmaceutical company” · word for word
16 Jun 20268-K · 8.01Annual Rent $300,000.00open
Figures in the filing · each found in the filing text
| Annual Rent · annual | $300000.00 |
Risks flagged
Relocation execution risk; potential disruption.
“plans to relocate its corporate headquarters” · word for word
13 May 202610-QNet Loss $-23M (+15% y/y); Cash, Cash Equivalents, Restricted Cash and Short-term Investments $332M; Net Cash Used in Operating Activities $-21M (+24% y/y)open
Figures in the filing · each found in the filing text
| Net Loss · Q1-2026 | $-23M | +15% y/y |
| Cash, Cash Equivalents, Restricted Cash and Short-term Investments · 2026-03-31 | $332M | |
| Net Cash Used in Operating Activities · Q1-2026 | $-21M | +24% y/y |
| Net Cash Provided by Financing Activities · Q1-2026 | $78M | +130% y/y |
| Research and Development Expenses · Q1-2026 | $16M | +2% y/y |
| General and Administrative Expenses · Q1-2026 | $8M | +34% y/y |
| Interest Income · Q1-2026 | $3M | +88% y/y |
| Interest Expense · Q1-2026 | $1M | |
| Accumulated Deficit · 2026-03-31 | $672M | |
| Net Proceeds from January 2026 RDO · Q1-2026 | $70M |
Risks flagged
Tariff and Inflation Risk
“If the tariffs and counter tariffs continue or escalate, they could have a significant negative effect on the global economy or on our operations, including continued inflationary pressures on raw materials, supply chain and logistics disruptions, and volatility in the capital markets, foreign exchange rates and interest rates.” · word for word
Middle East Conflict Risk
“Should the conflict continue or escalate, it could have a significant negative effect on the global economy or on our operations, including continued inflationary pressures on raw materials, oil and energy prices and clinical trial costs, supply chain and logistics disruptions, volatility in foreign exchange rates and interest rates and heightened cybersecur” · word for word
Clinical Trial Risk
“We have not generated any revenues from the sale of any products to date, and there is no assurance of any future revenues from product sales.” · word for word
Financing Risk
“In order to address our capital needs, including our planned clinical trials, we must continue to actively pursue additional equity or debt financing, and monetization of our existing programs through partnership arrangements or sales to third parties.” · word for word
13 May 20268-K · 2.02Cash, cash equivalents and short-term investments $332M; Net loss $-23M; Net loss per share $-0.18earningsopen
Figures in the filing · each found in the filing text
| Cash, cash equivalents and short-term investments · Q1-2026 | $332M | |
| Net loss · Q1-2026 | $-23M | |
| Net loss per share · Q1-2026 | $-0.18 | |
| Research and development expenses · Q1-2026 | $16M | |
| General and administrative expenses · Q1-2026 | $8M | |
| Interest income · Q1-2026 | $3M | |
| Gross proceeds from direct offering · Q1-2026 | $75M | |
| ATM proceeds · Q1-2026 | $9M | |
| Gross proceeds from public offering · Q2-2026 | $225M | |
| Cash, cash equivalents and short-term investments (April 30) · Q2-2026 | $535M |
Risks flagged
No material risk signals; pre-revenue biotech with clinical trial execution risk.
24 Apr 20268-K · 1.01Altimmune, Inc. enters underwriting agreement to issue 64.25M shares of common stock and pre-funded warrants at $3.00/share, raising ~$211.2M net proceeds to fund Phase 3 MASH trial of pemvidutide and pre-commercial activities.open
Figures in the filing · each found in the filing text
| Shares offered (common stock) · 2026-04-22 | 64,250,000 | |
| Pre-funded warrants offered · 2026-04-22 | 10,750,000 | |
| Public offering price per share · 2026-04-22 | $3.00 | |
| Net proceeds · 2026-04-24 | $211M | |
| Common Stock Warrant exercise price · 2026-04-22 | $3.00 |
Risks flagged
Significant dilution from offering; warrants could further dilute if exercised.
“64,250,000 shares ... and ... pre-funded warrants ... to purchase up to 10,750,000 shares”
Clinical trial risk: Phase 3 MASH trial may fail, rendering capital deployment unsuccessful.
“to continue to advance the clinical development of pemvidutide, including funding and preparation for its global pivotal Phase 3 trial in MASH” · word for word
17 Mar 2026DEF 14ANet Loss $-88M; Total Shareholder Return (TSR) 21.95open
Figures in the filing · each found in the filing text
| Net Loss · FY2025 | $-88M | |
| Total Shareholder Return (TSR) · FY2025 | 21.9% |
Risks flagged
Clinical trial failure risk
“The Company is a clinical-stage biopharmaceutical company with no approved products and a history of net losses. Pemvidutide is in Phase 2/3 and may fail to meet endpoints or gain regulatory approval.”
Capital needs risk
“The Company is seeking to increase authorized shares from 200M to 400M to facilitate future capital raises, indicating ongoing dilution risk.”
6 Mar 202610-KRevenue $41,000.00 (+105% y/y); Net Loss $-88M (-7% y/y); Research and Development Expenses $66M (-19% y/y); Guidance: Cash sufficient for at least 12 monthsopen
Figures in the filing · each found in the filing text
| Revenue · FY2025 | $41000.00 | +105% y/y |
| Net Loss · FY2025 | $-88M | -7% y/y |
| Research and Development Expenses · FY2025 | $66M | -19% y/y |
| General and Administrative Expenses · FY2025 | $28M | +34% y/y |
| Cash, Cash Equivalents, Restricted Cash and Short-term Investments · FY2025 | $274M | |
| Accumulated Deficit · FY2025 | $-650M | |
| Net Cash Used in Operating Activities · FY2025 | $-68M | -15% y/y |
| Net Cash Provided by Financing Activities · FY2025 | $207M | +1958% y/y |
| ATM Proceeds (Net) · FY2025 | $173M | |
| Term Loan Proceeds (Net) · FY2025 | $34M |
Guidance
Cash sufficient for at least 12 months
Company reaffirms cash runway of at least 12 months. Plans to increase R&D spend for Phase 3 MASH trial and other indications.
Risks flagged
No product revenue and history of losses
“We have not generated any revenue from the sale of any products to date. We have incurred significant losses since we commenced operations. As of December 31, 2025, we had an accumulated deficit of $649.5 million.” · word for word
Dependence on future capital raises
“In order to address our capital needs, including our planned clinical trials, we must continue to actively pursue additional equity or debt financing, and monetization of our existing programs through partnership arrangements or sales to third parties.” · word for word
Clinical trial execution risk
“The successful development of our product candidates is highly uncertain and may never result in approved products.” · word for word
Regulatory approval risk
“if the FDA, or another regulatory authority were to require us to conduct clinical trials beyond those that we currently anticipate will be required for the completion of clinical development of a product candidate, we could be required to expend significant additional financial resources and time on the completion of clinical development.” · word for word
5 Mar 20268-K · 2.02Cash, cash equivalents and short-term investments $274Mearningsopen
Figures in the filing · each found in the filing text
| Cash, cash equivalents and short-term investments · Q4-2025 | $274M |
Risks flagged
Clinical trial risk; no approved products or revenue
“Pre-revenue biotech; Phase 3 MASH trial not yet initiated; AUD trial data expected Q3 2026”
28 Jan 20268-K · 1.01Altimmune entered a securities purchase agreement and issued pre-funded warrants, indicating a capital raise via equity offering.open
Risks flagged
Dilution risk from pre-funded warrants; no specific financial terms disclosed in this filing.
“Pre-Funded Warrant exhibit indicates potential future equity dilution.”
19 Dec 20258-K · 7.01, 8.01ELF score change (1.8mg) -0.58; LSM change (1.8mg) -3.97; Proportion of patients with ≥0.5 ELF reduction (1.8mg) 32.4open
Figures in the filing · each found in the filing text
| ELF score change (1.8mg) · Q4-2025 | $-0.58 | |
| LSM change (1.8mg) · Q4-2025 | $-3.97 | |
| Proportion of patients with ≥0.5 ELF reduction (1.8mg) · Q4-2025 | 32.4% | |
| Proportion of patients with ≥30% LSM reduction (1.8mg) · Q4-2025 | 27.8% |
Risks flagged
Clinical trial risk; Phase 3 may not replicate results.
“Forward-looking statements caution about risks and uncertainties.”
1 Dec 20258-K · 5.02, 7.01Reported the departure of a director or principal officer (CEO/CFO change); issued a Regulation FD disclosure (forward guidance or material update)open
Risks flagged
Clinical and regulatory risks for pemvidutide; CEO transition execution risk.
“risks relating to: delays in regulatory review, manufacturing and supply chain interruptions, access to clinical sites, enrollment, adverse effects on healthcare systems and disruption of the global economy; the reliability of the results of studies relating to human safety and possible adverse effects resulting from the administration of the Company's produ” · word for word
6 Nov 202510-QAltimmune reported Q3 2025 results with net loss improvement and positive Phase 2b MASH data.earningsopen
Figures in the filing · each found in the filing text
| Cash, cash equivalents, restricted cash and short-term investments · Q3-2025 | $211M | |
| Net loss · Q3-2025 | $-19M | -17% y/y |
| Interest income · Q3-2025 | $2M | +27% y/y |
| Net cash used in operating activities · 9M-2025 | $-48M | -22% y/y |
| Net cash provided by financing activities · 9M-2025 | $126M | |
| Accumulated deficit · Q3-2025 | $-622M |
Risks flagged
Tariff and trade policy risk
“If the tariffs and counter tariffs continue or escalate, they could have a significant negative effect on the global economy or on our operations, including continued inflationary pressures on raw materials, supply chain and logistics disruptions, and volatility in the capital markets, foreign exchange rates and interest rates.” · word for word
Government shutdown risk
“If the shutdown continues for a prolonged period of time, it could result in significant delays in the SEC’s and FDA's ability to timely review and process any submissions we have filed or may file or cause other regulatory delays, which could have a material adverse effect on our business.” · word for word
Clinical trial failure risk
“We have not generated any revenues from the sale of any products to date and there is no assurance of any future revenues from product sales.” · word for word
6 Nov 20258-K · 1.01, 2.02, 2.03Cash, cash equivalents and short-term investments $211M; Term loan availability $125Mopen
Figures in the filing · each found in the filing text
| Cash, cash equivalents and short-term investments · Q3-2025 | $211M | |
| Term loan availability | $125M |
Risks flagged
Debt service obligations and milestone-dependent funding
“Loan bears interest at 9.70% or prime+2.45%; third and fourth tranches subject to milestone achievement and lender approval.”
6 Nov 20258-K · 1.01, 1.02Aggregate offering price $200Mopen
Figures in the filing · each found in the filing text
| Aggregate offering price | $200M |
Risks flagged
Dilution risk from potential share sales
“Up to $200M in shares may be sold, increasing share count.”
Altimmune, Inc. — questions
- What did Altimmune, Inc. file recently?
- 18 SEC filings in the last 12 months. Latest: 8-K on 2026-09-29 — Appointment of Richard Menziuso as VP, Global Controller and Principal Accounting Officer, effective September 29, 2026. Routine executive hire with no material financial impact.
Every figure on this page comes from Altimmune, Inc.'s own SEC filings — see them on SEC EDGAR. Price data is licensed and shown only inside the product.
How these figures are read: methodology · EquiReason.