Last reviewed · How we verify
TEV-48125 - 3
At a glance
| Generic name | TEV-48125 - 3 |
|---|---|
| Also known as | monoclonal antibody |
| Sponsor | Teva Branded Pharmaceutical Products R&D, Inc. |
| Modality | Small molecule |
| Phase | Phase 1 |
Approved indications
Common side effects
- Injection site pain
- Injection site induration
- Injection site erythema
- Nasopharyngitis
- Upper respiratory tract infection
- Injection site pruritus
- Injection site haemorrhage
- Sinusitis
- Influenza
- Bronchitis
- Urinary tract infection
- Migraine
Key clinical trials
- A Randomized, Double-Blind, Placebo-Controlled Study With an Open-Label Period on Efficacy and Safety of Fremanezumab in Chinese Adults With Migraine (PHASE3)
- Fremanezumab Compassionate Use Program for Pediatric Patients
- Long-term Safety and Tolerability of Subcutaneous Administration of TEV-48125 for the Preventive Treatment of Migraine (PHASE3)
- A Study to Test if Fremanezumab Reduces Headache in Participants With Posttraumatic Headache (PTH) (PHASE2)
- To Assess Pharmacokinetics, Safety and Tolerability of TEV-48125 in Japanese and Caucasian Healthy Subjects After a Single Subcutaneous (SC) Administration of TEV-48125 (PHASE1)
- Comparing Efficacy and Safety of 2 Dose Regimens of Subcutaneous Administration of TEV-48125 Versus Placebo for the Preventive Treatment of Chronic Migraine (PHASE3)
- An Efficacy and Safety Study of Fremanezumab in Adults With Migraine (PHASE3)
- Efficacy and Safety of 2 Dose Regimens of TEV-48125 Versus Placebo for the Preventive Treatment of Episodic Migraine (PHASE3)
Primary sources
Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.
| Source | Used for |
|---|---|
| ClinicalTrials.gov | Trial enrolment, design, endpoints, results |