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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

ALTAltimmune, Inc.Follow ALT — free
Biotechnology · Healthcare
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Market cap
412.4M
P/E TTM
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Dividend yield
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52-week
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Next earnings
10 Nov, in 17 days

Every filing, read

last 12 months · SEC

What happened, the numbers inside, guidance and risks. The original is one click away.

29 Sep 20268-K · 5.02Appointment of Richard Menziuso as VP, Global Controller and Principal Accounting Officer, effective September 29, 2026. Routine executive hire with no material financial impact.SEC ↗
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%”
Read the original on SEC EDGAR ↗
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
Read the original on SEC EDGAR ↗
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 2464.4%
2-level Reduction in WHO-RDL - Placebo · placebo · Week 2434.8%
Zero HDD in Week 21-24 - Pemvidutide · pemvidutide 2.4 mg · Week 21-2442.2%
Zero HDD in Week 21-24 - Placebo · placebo · Week 21-2417.4%
Change from baseline in Percent of Days with Abstinence (LS mean) - Pemvidutide · pemvidutide 2.4 mg · Week 2438.9%
Change from baseline in Percent of Days with Abstinence (LS mean) - Placebo · placebo · Week 2420.5%

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
Read the original on SEC EDGAR ↗
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
Read the original on SEC EDGAR ↗
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
Read the original on SEC EDGAR ↗
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.

Read the original on SEC EDGAR ↗
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) · 2026-04-2264,250,000
Pre-funded warrants offered · 2026-04-2210,750,000
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
Read the original on SEC EDGAR ↗
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) · FY202521.9%

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.”
Read the original on SEC EDGAR ↗
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
Read the original on SEC EDGAR ↗
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”
Read the original on SEC EDGAR ↗
3 Feb 20268-K · 8.01Disclosed a material event under other events (litigation, recall, contract loss, or major announcement)SEC ↗
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.”
Read the original on SEC EDGAR ↗
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) · Q4-202532.4%
Proportion of patients with ≥30% LSM reduction (1.8mg) · Q4-202527.8%

Risks flagged

Clinical trial risk; Phase 3 may not replicate results.

“Forward-looking statements caution about risks and uncertainties.”
Read the original on SEC EDGAR ↗
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
Read the original on SEC EDGAR ↗
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
Read the original on SEC EDGAR ↗
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.”
Read the original on SEC EDGAR ↗
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.”
Read the original on SEC EDGAR ↗

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.