Product Description
Tanezumab is a humanized monoclonal IgG2 antibody that blocks NGF from activating trkA receptors on nociceptive neurons. (Sourced from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6069623/)
Mechanisms of Action: NGF Inhibitor
Novel Mechanism: Yes
Modality: Antibody
Route of Administration: Intravenous,Subcutaneous
FDA Designation: None *
Approval Status: Not Approved
Approved Countries: European Medicines Agency
Approved Indications: None
Known Adverse Events: None
Company: Pfizer
Company Location: NEW YORK NY 10017
Company CEO: Albert Bourla
Additonal Commercial Interests: None
Clinical Description
Countries in Clinic: Japan, United States
Active Clinical Trial Count: 2
Highest Development Phases
Phase 3: Musculoskeletal Pain
Phase 2: Neurilemmoma|Neurofibromatoses
Trial |
Phase |
Trial Status |
Disease |
Primary Completion Date |
Probability of Success |
---|---|---|---|---|---|
2019P003201 | P2 |
Active, not recruiting |
Neurofibromatoses|Neurilemmoma |
2022-09-30 |
|
JapicCTI-163141 | P3 |
Active |
Musculoskeletal Pain |
None |