Ozmosi | Hydromorphone Drug Profile
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Hydromorphone

Alternative Names: hydromorphone, dilaudid, hydromorphonhydrochlorid, palladone, exalgo
Clinical Status: Inactive
Latest Update: 2026-02-05
Latest Update Note: Clinical Trial Update

Product Description

Hydromorphone is used to relieve pain. Hydromorphone extended-release tablets are used to relieve severe pain in people who are expected to need pain medication around the clock for a long time and who cannot be treated with other medications.

Mechanisms of Action: OPRD Agonist, OPRK Agonist, OPRM Agonist

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Oral, Intravenous

FDA Designation: *

Approval Status: Approved

Approved Countries: Australia | Austria | Belgium | Brazil | Canada | Chile | Croatia | Czech | Denmark | Egypt | Estonia | Finland | France | Germany | Hungary | Iceland | Indonesia | Ireland | Italy | Japan | Korea | Latvia | Lithuania | Luxembourg | Mexico | Netherlands | New Zealand | Norway | Portugal | Saudi Arabia | Serbia | Slovakia | Slovenia | South Africa | Spain | Sweden | Switzerland | Taiwan | Turkey | United Kingdom | United States

Approved Indications: None

Known Adverse Events: None

Company: Johnson & Johnson
Company Location: Eastern America
Company CEO: Joaquin Duato
Additional Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Hydromorphone

Countries in Clinic: United States

Active Clinical Trial Count: 1

Recent & Upcoming Milestones

Highest Development Phases

Phase 3: Acute Pain|Morphine Dependence|Pain, Postoperative

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

NCT04606264

STUDY19030022

P3

Completed

Acute Pain|Morphine Dependence|Pain, Postoperative

2025-03-21

2025-10-23