Active Ingredient History
Tapentadol is the first US FDA-approved centrally acting analgesic having both μ-opioid receptor agonist and noradrenaline (norepinephrine) reuptake inhibition activity with minimal serotonin reuptake inhibition. Tapentadol is indicated for the management of pain severe enough to require daily, around-the-clock, long-term opioid treatment and for which alternative treatment options are inadequate, neuropathic pain associated with diabetic peripheral neuropathy (DPN) severe enough to require daily, around-the-clock, long-term opioid treatment and for which alternative treatment options are inadequate. NCATS
Drug Pricing (per unit)
Note: This drug pricing data is preliminary, incomplete, and may contain errors.
Organization | Org Type | FDA approvals | Clinical Trials involvement | Org ID | Force Sort |
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Organization | Org Type | FDA approvals | Clinical Trials involvement | Org ID | Force Sort |
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Acute Pain (Phase 4)
Analgesics, Opioid (Phase 4)
Arthralgia (Phase 3)
Arthritis (Phase 3)
Arthroplasty (Phase 3)
Back Pain (Phase 4)
Bone Diseases (Phase 2)
Bunion (Phase 3)
Chronic Pain (Phase 3)
Diabetes Mellitus (Phase 3)
Diabetic Neuropathies (Phase 3)
Hallux Valgus (Phase 3)
Healthy Volunteers (Phase 1)
Heart (Phase 1)
Hyperalgesia (Phase 1)
Hysterectomy (Phase 3)
Intestinal Neoplasms (Phase 4)
Joint Diseases (Phase 3)
Low Back Pain (Phase 4)
Neoplasms (Phase 3)
Neuralgia (Phase 4)
Neuralgia, Postherpetic (Phase 2)
Nociceptive Pain (Phase 3)
Osteoarthritis (Phase 3)
Osteoarthritis, Hip (Phase 3)
Osteoarthritis, Knee (Phase 4)
Pain ()
Pain Measurement (Phase 3)
Pain, Postoperative (Phase 4)
Peripheral Nervous System Diseases (Phase 4)
Pharmacokinetics (Phase 1)
Postoperative Complications (Phase 3)
Sciatica (Phase 3)
Tapentadol (Phase 3)
Visceral Pain (Phase 4)
Trial | Phase | Start Date | Organizations | Indications |
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