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Heron Therapeutics, Inc. (HRTX) SEC Filings & Earnings Calls

EquiReason read 16 Heron Therapeutics, Inc. SEC filings in the last 12 months. Latest: 8-K on 2026-09-29 — Heron Therapeutics entered a multi-product Development and License Agreement with Long Grove Pharmaceuticals and Capstone Development Services to import, distribute, sell and marke.

Source: SEC EDGAR filings · figures as of 2026-06-30 · read by EquiReason

HRTXHeron Therapeutics, Inc.Follow HRTX — free
Biotechnology · Healthcare
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Market cap
57.5M
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 · 1.01Heron Therapeutics entered a multi-product Development and License Agreement with Long Grove Pharmaceuticals and Capstone Development Services to import, distribute, sell and market certain products in the US. Includes regulatory and salesopen

Risks flagged

License agreement terms not fully disclosed; milestone and royalty payments may be material.

“Company shall pay regulatory milestone payments, sales-based milestone payments, and royalty payments.”
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14 Aug 20268-K · 1.01, 3.03Amendment to Tax Benefit Preservation Plan extending expiration date from 2026 to 2029; routine rights plan modification.open

Risks flagged

NOL preservation plan extension indicates company has significant tax attributes to protect; no immediate risk.

“Tax Benefit Preservation Plan extended to 2029.”
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10 Aug 202610-QCINVANTI patents invalidated in court; SUSTOL to be discontinuedopen

Risks flagged

Patent invalidation risk for CINVANTI

“On June 1, 2026, the U.S. District Court for the District of Delaware issued a decision ... holding that the asserted claims of Company’s U.S. Patent Nos. 12,115,255 and 12,290,520 are invalid under 35 U.S.C. § 112.” · word for word

Product discontinuation (SUSTOL)

“On June 15, 2026, we submitted a notification to the FDA that SUSTOL will no longer be available for sale as of September 30, 2026.” · word for word
Read the original on SEC EDGAR ↗
10 Aug 20268-K · 2.02Total net revenue $38M (+1% y/y); Cash, cash equivalents and short-term investments $43M; ZYNRELEF net revenue $11M (+35% y/y); Guidance: Withdrew full-year 2026 guidance for net product sales and Adjusted EBITDAearningsopen

Figures in the filing · each found in the filing text

Total net revenue · Q2-2026$38M+1% y/y
Cash, cash equivalents and short-term investments · Q2-2026$43M
ZYNRELEF net revenue · Acute Care · Q2-2026$11M+35% y/y
CINVANTI net revenue · Oncology · Q2-2026$22M-10% y/y
SUSTOL net revenue · Oncology · Q2-2026$540000.00-78% y/y
Acute Care net revenue · Acute Care · Q2-2026$15M+44% y/y
Oncology net revenue · Oncology · Q2-2026$22M-16% y/y

Guidance

Withdrew full-year 2026 guidance for net product sales and Adjusted EBITDA

Company withdrew full-year 2026 guidance due to patent litigation risk on CINVANTI, paused sales force expansion, and is considering strategic alternatives.

Risks flagged

Patent litigation risk on CINVANTI could lead to generic entry, significantly impacting the largest product's revenue.

“following the June 2026 decision of the U.S. District Court for the District of Delaware (the “Court”) regarding certain patents covering CINVANTI®, the Company does not believe it can reliably forecast the timing or terms of potential generic entry with respect to its largest product.” · word for word

Strategic alternatives process creates uncertainty; no timetable or assurance of transaction.

“the Company is considering strategic alternatives as it continues to execute its current plan. The Company has not set a timetable for this process, there can be no assurance that it will result in any transaction” · word for word
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25 Jun 20268-K · 3.01Received a delisting notice or transferred listing to another exchange; filed financial statements and exhibits with this reportopen

Risks flagged

Delisting risk due to low share price; potential reverse stock split needed.

“Nasdaq notice of non-compliance with minimum bid price requirement.”
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2 Jun 20268-K · 8.01Disclosed a material event under other events (litigation, recall, contract loss, or major announcement); filed financial statements and exhibits with this reportopen

Risks flagged

Loss of patent protection for CINVANTI could lead to generic competition and revenue decline.

“Court invalidated key patents; generic NDA filed by Slayback.”
Read the original on SEC EDGAR ↗
11 May 202610-QNet Product Sales $35M (-11% y/y); Gross Profit $24M (-21% y/y); Gross Margin 69.4open

Figures in the filing · each found in the filing text

Net Product Sales · Q1-2026$35M-11% y/y
Gross Profit · Q1-2026$24M-21% y/y
Gross Margin · Q1-202669.4%
Net Income (Loss) · Q1-2026$-8M
Operating Cash Flow · Q1-2026$-2M+83% y/y
Free Cash Flow · Q1-2026$-2M
Cash, Cash Equivalents and Short-term Investments · 2026-03-31$45M

Risks flagged

Oncology Revenue Decline

“Total oncology net product sales decreased by $7.5 million or 26.3% during the three months ended March 31, 2026, as compared to the comparable period in 2025.” · word for word

Accumulated Deficit

“We have incurred significant operating losses and negative cash flows from operations and had an accumulated deficit of $1.9 billion as of March 31, 2026.” · word for word

Gross Margin Pressure

“Gross profit for the three months ended March 31, 2026 was 69.4%, compared to 78.3% for the comparable period in 2025.” · word for word
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11 May 20268-K · 2.02Total net revenue $35M (-11% y/y); Acute Care net revenue $14M (+32% y/y); ZYNRELEF net revenue $10M (+27% y/y); Guidance: FY2026 net revenue $173M-$183M, Adjusted EBITDA $10M-$20Mearningsopen

Figures in the filing · each found in the filing text

Total net revenue · Q1-2026$35M-11% y/y
Acute Care net revenue · Acute Care · Q1-2026$14M+32% y/y
ZYNRELEF net revenue · ZYNRELEF · Q1-2026$10M+27% y/y
APONVIE net revenue · APONVIE · Q1-2026$3M+50% y/y
Oncology net revenue · Oncology · Q1-2026$21M-26% y/y
CINVANTI net revenue · CINVANTI · Q1-2026$21M-20% y/y
SUSTOL net revenue · SUSTOL · Q1-2026$547000.00-81% y/y
Cash, cash equivalents and short-term investments · Q1-2026$45M

Guidance

FY2026 net revenue $173M-$183M, Adjusted EBITDA $10M-$20M

Full-year guidance reaffirmed; acute care growth strong; temporary margin pressure expected to normalize.

Risks flagged

Oncology franchise decline (CINVANTI -20%, SUSTOL wind-down)

“Oncology net revenue decreased 26.3% YoY; SUSTOL being wound down by end of 2026.”

Temporary gross margin pressure from higher-cost inventory

“expect temporary gross margin pressure to normalize as we work through higher-cost CINVANTI inventory over the next two quarters.” · word for word
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30 Apr 2026DEF 14AProxy statement for annual meeting; discloses executive compensation tied to financial and operational goals, significant insider ownership by Rubric and Velan, and proposals to increase equity plan shares and ratify a tax benefits preservaopen

Figures in the filing · each found in the filing text

Total Net Revenue · FY2025$155M
ZYNRELEF and APONVIE revenue · FY2025$50M
CINVANTI and SUSTOL revenue · FY2025$105M
Operating Expense · FY2025$103M
EBITDA · FY2025$15M
Cash on hand · FY2025$47M
Federal NOL carryforwards · FY2025$1.30B
State NOL carryforwards · FY2025$900M

Risks flagged

NOL impairment risk

“The federal NOL carryforwards consist of $541.7 million generated before January 1, 2018, which began to expire in 2025, and $793.9 million that can be carried forward indefinitely, but are subject to the 80% taxable income limitation.” · word for word

Ownership change risk

“the beneficial ownership of the Company’s common stock...held by certain of the Company’s existing investors, has increased, which has increased the risk of an ownership change under Section 382 of the Internal Revenue Code” · word for word
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6 Apr 20268-K · 5.02Reported the departure of a director or principal officer (CEO/CFO change); filed financial statements and exhibits with this reportopen

Risks flagged

Potential retention risk if executives leave; enhanced severance could be costly.

“Enhanced severance payments and equity acceleration in change-in-control scenarios.”
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26 Feb 20268-K · 2.02Total Net Revenue $155M (+7% y/y); Acute Care Net Revenue $50M (+65% y/y); ZYNRELEF Net Revenue $38M (+49% y/y); Guidance: FY2026 net revenue guidance $173-$183M vs FY2025 actual $154.9M; adjusted EBITDA $10-$20M.earningsopen

Figures in the filing · each found in the filing text

Total Net Revenue · FY2025$155M+7% y/y
Acute Care Net Revenue · Acute Care · FY2025$50M+65% y/y
ZYNRELEF Net Revenue · Acute Care · FY2025$38M+49% y/y
APONVIE Net Revenue · Acute Care · FY2025$12M+156% y/y
Oncology Net Revenue · Oncology · FY2025$105M-8% y/y
CINVANTI Net Revenue · Oncology · FY2025$97M-3% y/y
SUSTOL Net Revenue · Oncology · FY2025$9M-40% y/y
Cash and Short-Term Investments · Q4-2025$47M

Guidance

FY2026 net revenue guidance $173-$183M vs FY2025 actual $154.9M; adjusted EBITDA $10-$20M.

Strong guidance raise reflecting Acute Care franchise momentum and improving profitability.

Risks flagged

Oncology franchise revenue decline of 7.8% YoY, driven by SUSTOL (-39.9%) and CINVANTI (-3.3%).

“Oncology $105,261k vs $114,221k, -7.8% decrease”

Dependence on Acute Care franchise for growth; competitive and reimbursement risks.

“Acute Care franchise growth driven by ZYNRELEF and APONVIE; J-Code approvals support reimbursement.”
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26 Feb 202610-KNet product sales $155M (+7% y/y); Acute Care Net Product Sales $50M (+65% y/y); Oncology Net Product Sales $105M (-8% y/y)open

Figures in the filing · each found in the filing text

Net product sales · FY2025$155M+7% y/y
Acute Care Net Product Sales · Acute Care · FY2025$50M+65% y/y
Oncology Net Product Sales · Oncology · FY2025$105M-8% y/y
Gross Profit · FY2025$114M+8% y/y
Cash, cash equivalents and short-term investments · 2025-12-31$47M
Net loss · FY2025$-20M+49% y/y
Net cash used in operating activities · FY2025$-28M+23% y/y

Risks flagged

Patent litigation risk

“While in December 2024, the District Court found that the Company’s CINVANTI patents are valid and would be infringed by Fresenius Kabi’s proposed generic product, this decision is currently pending appeal and there is no guarantee that other similar or future litigation will be resolved in our favor.” · word for word

Debt burden

“As of December 31, 2025, $111.2 million in aggregate principal amount, including accumulated paid-in-kind interest, under the Working Capital Facility Agreement were outstanding... As of December 31, 2025, $35.9 million aggregate principal amount, including accumulated paid-in-kind interest, for the 2031 Convertible Notes was outstanding.” · word for word

Activist stockholder risk

“In August 2025, we entered into a Cooperation Agreement with Rubric Capital Management LP, regarding certain changes to the composition of the Board and other related matters.” · word for word
Read the original on SEC EDGAR ↗
9 Jan 20268-K · 7.01Net revenue $40M; ZYNRELEF net revenue $12M; APONVIE net revenue $4Mopen

Figures in the filing · each found in the filing text

Net revenue · Q4-2025$41M
ZYNRELEF net revenue · Acute Care · Q4-2025$13M
APONVIE net revenue · Acute Care · Q4-2025$4M
CINVANTI net revenue · CINV · Q4-2025$23M
SUSTOL net revenue · CINV · Q4-2025$1M
Net revenue · FY2025$155M

Risks flagged

Preliminary results subject to audit adjustment.

“Preliminary, unaudited net revenue; final results may differ.”
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4 Nov 202510-QHeron Therapeutics reported Q3 2025 net product sales +16.5% YoY, with acute care surging 67% but oncology declining; net loss widened to $17.5M due to debt extinguishment costs.earningsopen

Figures in the filing · each found in the filing text

Net product sales · Q3-2025$38M+17% y/y
Net income (loss) · Q3-2025$-18M
Acute care net product sales · Acute Care · Q3-2025$12M+67% y/y
Oncology net product sales · Oncology · Q3-2025$26M+2% y/y
Gross profit margin · Q3-202568.8%
Cash, cash equivalents and short-term investments · 2025-09-30$56M
Accumulated deficit · 2025-09-30$1.90B
Net cash used in operating activities · 9M-2025$-18M

Risks flagged

Oncology revenue decline due to competition

“Total oncology net product sales decreased 3.4% or $2.8 million during the nine months ended September 30, 2025, as compared to the comparable period in 2024. The decrease was primarily attributable to market competition from branded products and generics.” · word for word

SUSTOL wind-down and potential reintroduction uncertainty

“We intend to wind down commercialization of SUSTOL over the next 12 months while we evaluate potential product updates.” · word for word

High accumulated deficit and net loss

“We have incurred significant operating losses and negative cash flows from operations and had an accumulated deficit of $1.9 billion as of September 30, 2025.” · word for word

Loss on debt extinguishment from refinancing

“The increase in expense is related to the loss on debt extinguishment of $11.3 million and an increase in interest expense as a result of the debt refinancing completed in 2025.” · word for word
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4 Nov 20258-K · 2.02Net Revenue $38M (+16% y/y); SUSTOL Net Revenue $2M (-31% y/y); Cash, cash equivalents, and short-term investments $56M; Guidance: Net Revenue $153M-$163M; Adjusted EBITDA $9M-$13Mearningsopen

Figures in the filing · each found in the filing text

Net Revenue · Q3-2025$38M+17% y/y
SUSTOL Net Revenue · Oncology · Q3-2025$2M-31% y/y
Cash, cash equivalents, and short-term investments · 2025-09-30$56M

Guidance

Net Revenue $153M-$163M; Adjusted EBITDA $9M-$13M

Reaffirmed full-year 2025 guidance; adjusted EBITDA guidance raised from earlier range; strong commercial momentum.

Risks flagged

Dependence on commercial execution for ZYNRELEF and APONVIE; oncology segment SUSTOL declining

“SUSTOL revenue declined 30.8% YoY; oncology segment overall flat; guidance still wide range.”
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29 Oct 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

Activist investor influence may lead to strategic changes or pressure.

“Cooperation Agreement with Rubric Capital Management LP; director with activist background.”
Read the original on SEC EDGAR ↗

Heron Therapeutics, Inc. — questions

What did Heron Therapeutics, Inc. file recently?
16 SEC filings in the last 12 months. Latest: 8-K on 2026-09-29 — Heron Therapeutics entered a multi-product Development and License Agreement with Long Grove Pharmaceuticals and Capstone Development Services to import, distribute, sell and market certain products in the US. Includes regulatory and sales

Every figure on this page comes from Heron Therapeutics, 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.