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Heron Therapeutics, Inc.

Heron Therapeutics, Inc. logo
🇺🇸United States
Ownership
Public
Established
1983-01-01
Employees
126
Market Cap
$292.7M
Website
http://www.herontx.com

Clinical Trials

28

Active:3
Completed:23

Trial Phases

4 Phases

Phase 1:2
Phase 2:12
Phase 3:6
+1 more phases

Drug Approvals

12

FDA:4
CANADA:4

Drug Approvals

ZYNRELEF

Approval Date
May 30, 2025
FDA

APONVIE

Approval Date
Mar 13, 2024
FDA

CINVANTI

Approval Date
Mar 13, 2024
FDA

SUSTOL

Approval Date
Jun 7, 2023
FDA

Clinical Trials

Distribution across different clinical trial phases (26 trials with phase data)• Click on a phase to view related trials

Phase 2
12 (46.2%)
Phase 3
6 (23.1%)
Phase 4
6 (23.1%)
Phase 1
2 (7.7%)

A Multi-surgery Assessment of ZYNRELEF (HTX-011), AMAZE.

Phase 4
Completed
Conditions
Total Shoulder Arthroplasty
Multimodal Analgesia
Postoperative Pain
Interventions
First Posted Date
2023-10-31
Last Posted Date
2023-10-31
Lead Sponsor
Heron Therapeutics
Target Recruit Count
30
Registration Number
NCT06109415
Locations
🇺🇸

Woodland International Research Group, LLC, Little Rock, Arkansas, United States

🇺🇸

Center for Orthopaedic Reconstruction and Excellence, Jenks, Oklahoma, United States

🇺🇸

First Surgical Hospital, Bellaire, Texas, United States

and more 2 locations

A Multi-surgery Assessment of ZYNRELEF (HTX-011), AMAZE

Phase 4
Completed
Conditions
Analgesia
Interventions
First Posted Date
2023-10-31
Last Posted Date
2023-10-31
Lead Sponsor
Heron Therapeutics
Target Recruit Count
30
Registration Number
NCT06109428
Locations
🇺🇸

First Surgical Hospital, Bellaire, Texas, United States

🇺🇸

Endeavor Clinical Trials, LLC, San Antonio, Texas, United States

Safety Study of Repeat Doses of SUSTOL in Adults

Phase 4
Active, not recruiting
Conditions
Chemotherapy-Induced Nausea and Vomiting (CINV)
Interventions
First Posted Date
2022-06-28
Last Posted Date
2023-07-28
Lead Sponsor
Heron Therapeutics
Target Recruit Count
300
Registration Number
NCT05434663
Locations
🇺🇸

Hattiesburg Clinic Hematology/Oncology, Hattiesburg, Mississippi, United States

🇺🇸

Gabrail Cancer Center Research, Canton, Ohio, United States

A Multi-surgery Assessment of ZYNRELEF (HTX-011), AMAZE. Master Protocol HTX-011-401.

Phase 4
Active, not recruiting
Conditions
Analgesia
Interventions
First Posted Date
2021-11-05
Last Posted Date
2023-10-26
Lead Sponsor
Heron Therapeutics
Target Recruit Count
90
Registration Number
NCT05109312
Locations
🇺🇸

Woodland International Research Group, LLC, Little Rock, Arkansas, United States

🇺🇸

Gulfcoast Research Institute, Sarasota, Florida, United States

🇺🇸

The Orthopaedic Center, Tulsa, Oklahoma, United States

and more 4 locations

HTX-011 in Spinal Surgery

Phase 2
Completed
Conditions
Post-Operative Pain
Lumbar Laminectomy
Interventions
First Posted Date
2021-06-02
Last Posted Date
2023-06-12
Lead Sponsor
Heron Therapeutics
Target Recruit Count
32
Registration Number
NCT04911062
Locations
🇺🇸

Arizona Research Center, Phoenix, Arizona, United States

🇺🇸

Lotus Clinical Research, LLC, Pasadena, California, United States

🇺🇸

Kansas Spine and Specialty Hospital, Wichita, Kansas, United States

and more 9 locations
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News

Heron Therapeutics Settles Patent Litigation with Mylan for CINVANTI and APONVIE

Heron Therapeutics has reached a settlement agreement with Mylan Pharmaceuticals to resolve ongoing patent litigations related to CINVANTI and APONVIE injectable emulsions.

Design Therapeutics Appoints Dr. Chris Storgard as Chief Medical Officer to Advance GeneTAC® Pipeline

Design Therapeutics has appointed Chris Storgard, M.D., as Chief Medical Officer, bringing over two decades of leadership in drug development with experience advancing multiple assets through global regulatory approvals.

FDA Approves Heron Therapeutics' Zynrelef Vial Access Needle for Postoperative Pain Management

The FDA has approved Heron Therapeutics' Prior Approval Supplement Application for the Zynrelef Vial Access Needle (VAN).

FDA Nears Decisions on Vanda, Zevra, Heron, Merck, BMS, Sanofi/Regeneron

• Vanda Pharmaceuticals awaits FDA decision on tradipitant for gastroparesis, a condition affecting millions in the U.S., with a verdict expected by September 18. • Zevra Therapeutics anticipates potential approval of arimoclomol for Niemann-Pick disease type C (NPC) by September 21, following positive advisory committee support. • The FDA is set to decide on Heron Therapeutics' extended-release needle for Zynrelef by September 23, designed to simplify drug preparation and administration. • Merck seeks approval for Keytruda in pleural mesothelioma, with a decision due September 25, based on Phase II/III KEYNOTE-483 trial data showing improved survival. • Bristol Myers Squibb awaits FDA decision on KarXT for schizophrenia by September 26, potentially offering a novel mechanism of action targeting muscarinic receptors. • Sanofi and Regeneron anticipate a decision on Dupixent for COPD by September 27, supported by Phase III BOREAS and NOTUS trials demonstrating reduced exacerbations.

FDA Nears Decisions on Key Therapies for Gastroparesis, Niemann-Pick Disease, Schizophrenia, COPD, Mesothelioma, and Post-Surgical Pain

• The FDA is expected to decide on Vanda Pharmaceuticals' tradipitant for gastroparesis by September 18, potentially offering a novel NK-1R antagonist treatment option. • Zevra Therapeutics awaits a verdict by September 21 on arimoclomol for Niemann-Pick disease type C, an ultrarare neurodegenerative disorder with no approved therapies. • A decision is anticipated by September 26 on Bristol Myers Squibb's KarXT for schizophrenia, representing a new pharmacological approach targeting muscarinic receptors.

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