HYDROMORPHONE HYDROCHLORIDE (hydromorphone hydrochloride) by Pfizer is mµ-opioid receptor, although it can bind to other opioid receptors at higher doses. First approved in 2011.
Drug data last refreshed 4h ago · AI intelligence enriched 1w ago
Hydromorphone hydrochloride is a semi-synthetic opioid agonist administered via injection for acute and chronic pain management. It acts primarily on µ-opioid receptors in the CNS to produce analgesia, with no ceiling effect on analgesic potency. The drug is indicated for patients requiring parenteral opioid therapy when oral or other routes are not suitable.
Product is in peak commercial phase with established market presence; expect mature team structure and focus on market maintenance and competitive defense.
mµ-opioid receptor, although it can bind to other opioid receptors at higher doses. The principal therapeutic action of hydromorphone is analgesia. Like all full opioid agonists, there is no ceiling effect for analgesia with morphine. Clinically, dosage is titrated to provide adequate analgesia and…
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Single-arm Study to Assess the Safety of Hydromorphone Hydrochloride by Intrathecal Administration
Safety and Efficacy Study of Hydromorphone Hydrochloride by Intrathecal Administration
An Efficacy and Safety Study of Oral Osmotic Therapeutic System (OROS) Hydromorphone Hydrochloride (HCl) in Participants With Cancer Related Pain
A Study to Compare Safety and Efficacy of Osmotic Release Oral Syytem (OROS) Hydromorphone Hydrochloride (HCl) With Morphine Sustain Release (SR) in Participants With Cancer Pain
An Efficacy and Safety Study of Hydromorphone Hydrochloride (HCl) Oral Osmotic System (OROS) in the Reduction of Breakthrough Pain Medication Frequency in Participants With Cancer
Worked on HYDROMORPHONE HYDROCHLORIDE at Pfizer? Share your interview experience or compensation data (+7 days Pro)
The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.
Upgrade to Pro to access CMS Part B ASP pricing data and other premium pharma intelligence.
Upgrade to Pro — $25/moWorking on hydromorphone at peak lifecycle offers exposure to mature commercial execution, complex regulatory/safety compliance, and opioid-specific risk management in a highly scrutinized therapeutic class. Team size is likely stable with emphasis on market defense, payer management, and pharmacovigilance rather than launch activities.