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HRTXNasdaq

HERON THERAPEUTICS, INC. /DE/

Biopharma developer (SEC filing verified)·Commercial·Cary, NC, United States·CEO: Mr. Craig Alexander Collard
OncologyInfectious DiseasePainDermatologyPsychiatry

HRTX evidence brief

What we can confirm

BioSniper Score:
5.7 / 10
Market Cap:
$59.9M
Lead Asset:
cinvanti (Approved)

What it means

The company data is ready for cross-source review; unsupported conclusions remain unknown.

What to watch

Market Cap: $59.9M · Lead Asset: cinvanti (Approved)
BioSniper AIPage evidence connected

Prepared research question

What matters most for HRTX—catalysts, financial risk and supporting evidence?

Run cited research

Traceable citations · Unknowns marked

BioSniper AI · HRTX

HERON Therapeutics is a commercial-stage biopharmaceutical company focused on developing and marketing proprietary formulations of antiemetic drugs, primarily for chemotherapy-induced nausea and vomiting, with two approved products (CINVANTI and SUSTOL) and a limited pipeline.

Key risk: Ongoing net losses

5.7/10

BioSniper Score

Based on 4 of 6 signals

Market Cap

$59.9M

Cash Runway

—

Financial data as of Jun 30, 2026.

Tracking 3 pipeline candidates · 19 clinical trials · 1 catalyst · 4 FDA decisions for HERON THERAPEUTICS, INC. /DE/.

AI OverviewAI overview is shown in English only.

HERON Therapeutics is a commercial-stage biopharmaceutical company focused on developing and marketing proprietary formulations of antiemetic drugs, primarily for chemotherapy-induced nausea and vomiting, with two approved products (CINVANTI and SUSTOL) and a limited pipeline.

  • Cash and equivalents of $20.7M as of 2026-06-30 [sec]
  • Total revenue of $37.7M and net loss of -$5.5M for the six months ended June 30, 2026 [sec]
  • Two FDA-approved products: CINVANTI (aprepitant injectable emulsion) and SUSTOL (granisetron extended-release injection) for chemotherapy-induced nausea and vomiting [sec_mda · as of 2026-02-26]
  • SUSTOL commercialization is being wound down, with potential reintroduction as early as late 2027 [sec_mda · as of 2026-02-26]
  • Shareholders' equity of $6.9M as of 2026-06-30 [sec]

What works

  • Two approved products (CINVANTI and SUSTOL) provide a commercial revenue base in the antiemetic market [sec_mda · as of 2026-02-26]
  • Proprietary Biochronomer Technology platform enables extended-release formulations, as used in SUSTOL [sec_mda · as of 2026-05-11]
  • Management states cash, cash equivalents and short-term investments are sufficient for at least one year from the date of the May 2026 filing [sec_mda · as of 2026-05-11]

What to weigh

  • Net loss of -$5.5M on revenue of $37.7M for the six months ended June 30, 2026 indicates ongoing unprofitability [sec]
  • SUSTOL commercialization is being wound down, creating transition costs and revenue uncertainty [sec_mda · as of 2026-02-26]
  • Limited pipeline beyond the two approved products; no new clinical candidates are described in recent filings [pipeline]
  • Shareholders' equity of only $6.9M against $20.7M cash suggests a thin capital base [sec]

From the filings

Quoted directly from source documents.

  • SUSTOL wind-down and potential reintroduction

    “We intend to wind down commercialization of SUSTOL over the next 12 months while we evaluate potential product updates. Subject to development progress, manufacturing readiness, and regulatory feedback, we may consider reintroducing SUSTOL as early as late 2027.”

    SEC MD&A · February 26, 2026

  • Cash runway of at least one year

    “cash, cash equivalents and short-term investments will be sufficient to meet the Company's anticipated cash requirements for a period of at least one year from the issuance of the condensed consolidated financial statements”

    SEC MD&A · May 11, 2026

Catalyst timeline

  • 2035-09-18 · Patent_Expiry · APREPITANT — Patent_Expiry: NDA209296 — The patent for aprepitant (CINVANTI) expires, potentially allowing generic competition to enter the market.
Risks & what to watch (4)›

Key risks

  • Ongoing net losses — Net loss of -$5.5M on $37.7M revenue for H1 2026; company not yet profitable [sec]
  • SUSTOL wind-down uncertainty — Wind-down of SUSTOL commercialization with potential reintroduction only as early as late 2027; transition costs not yet quantified [sec_mda · as of 2026-02-26]
  • Thin capital base — Shareholders' equity of $6.9M against $20.7M cash; limited buffer against adverse events [sec]
  • Limited pipeline depth — No new clinical candidates described in recent filings; pipeline consists only of two approved products [pipeline]

What to watch

  • SUSTOL wind-down execution and quantification of one-time transition costs [sec_mda · as of 2026-02-26]
  • Potential reintroduction of SUSTOL as early as late 2027, subject to development, manufacturing, and regulatory feedback [sec_mda · as of 2026-02-26]
  • Cash runway and whether the company can achieve profitability before needing additional capital [sec_mda · as of 2026-05-11]
  • Patent expiry for APREPITANT (CINVANTI) on 2035-09-18, which could open generic competition [catalyst]

Sources: Catalysts · Pipeline · SEC MD&A · Generated October 11, 2026 · How we verify sources →

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Evidence & data

Score breakdownBased on 4 of 6 signals · derived from public data

Cash RunwayN/A

Cash runway data unavailable

Financial Health5.0

D/E 35.52 · 0% dilution

Pipeline Maturity10.0

Lead: Approved

Pipeline Breadth5.9

3 candidates

Catalyst Momentum2.0

1 upcoming, next in ~3261d

Insider SignalN/A

No insider transactions in the last 180 days

Catalysts

Pipeline

Regulatory

Financials

Institutional Holdings

Source: SEC Form 13F · as of Mar 2026

Institutional holders

167

Total value held

$125.0M

Showing top 10 of 167 institutional holders of HERON THERAPEUTICS, INC. /DE/. Open the full 13F history after sign-in.

Short Interest

as of Apr 20, 2026
% of float
25.7%
Days to cover
19.9
Shares short
39,421,430
Daily short volume
-

Short percent of float and days-to-cover reflect reported short positioning. Daily short volume is the exchange-reported short share of a single day's trading volume and is noisier. See the most-shorted biotech ranking →

HRTX short interest

Governance

Frequently asked questions

What is the AI investment thesis for HERON THERAPEUTICS, INC. /DE/?

HERON Therapeutics is a commercial-stage biopharmaceutical company focused on developing and marketing proprietary formulations of antiemetic drugs, primarily for chemotherapy-induced nausea and vomiting, with two approved products (CINVANTI and SUSTOL) and a limited pipeline.

What is HERON THERAPEUTICS, INC. /DE/'s lead drug candidate?

HERON THERAPEUTICS, INC. /DE/'s most advanced tracked candidate is cinvanti (Approved).

What is HERON THERAPEUTICS, INC. /DE/'s next catalyst?

HERON THERAPEUTICS, INC. /DE/'s next tracked catalyst is a Patent_Expiry event — "Patent_Expiry: NDA209296" — expected September 18, 2035.

Who is the CEO of HERON THERAPEUTICS, INC. /DE/?

Mr. Craig Alexander Collard is the chief executive officer of HERON THERAPEUTICS, INC. /DE/ (HRTX).

Where is HERON THERAPEUTICS, INC. /DE/ headquartered?

HERON THERAPEUTICS, INC. /DE/ (HRTX) is headquartered in Cary, NC, United States.

923 companies304,846 SEC filings22,720 clinical trials100% citation-verification pass rate (7d)How we verify →

The AI overview and BioSniper Score are neutral, data-derived signals built from public SEC filings, ClinicalTrials.gov and FDA records — not investment advice.