Eptinezumab
DrugEptinezumab will be administered per dose and schedule specified in the arm.
Other names: Vyepti
NCT Number: NCT04965675
To find out if eptinezumab is better than placebo (normal saline solution) in lowering the number of days with migraine in young people ages 12 to 17 with chronic migraine.
Interested in participating?
Request Info12 year–17 year
All sexes
Interventional
Phase 3
Hospital Privado de La Comunidad, Mar del Plata, Buenos Aires, Argentina
The study includes a single intravenous (IV) infusion of the study drug and consists of a screening period (4 weeks), a double-blind, placebo-controlled period (12 weeks), and a safety follow-up period (8 weeks). Participants confirmed eligible will be randomized (1:1:1) to receive a single IV infusion of either eptinezumab 300 milligrams (mg) dose (weight adjusted; targeting adult exposure after 300 mg IV), eptinezumab 100 mg (weight adjusted; targeting adult exposure after 100 mg IV), or placebo at randomization visit. The doses will be adjusted for the participant's body weight.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Eptinezumab will be administered per dose and schedule specified in the arm.
Other names: Vyepti
Placebo matching to eptinezumab will be administered per schedule specified in the arm.
Time frame: Baseline, Weeks 1-12
Time frame: Baseline up to Weeks 1-12
Time frame: Day 1
Time frame: Baseline, Weeks 1-12
Time frame: Baseline up to Weeks 1-12
Time frame: Baseline up to Weeks 1-4
Time frame: Baseline up to Weeks 1-4
Time frame: Baseline, Weeks 1-12
Time frame: Baseline, Weeks 1-12
Time frame: Baseline, Weeks 1-12
Time frame: Baseline, Weeks 1-12
Time frame: Randomization ( pre-dose [Week 0]), Week 8, Week 12, and safety follow up visit (Week 20)
Time frame: From randomization (Week 0) up to Week 20
Time frame: From randomization (Week 0) up to Week 20
Contact information is provided by the study sponsor or research team.
H. Lundbeck A/S
Industry
Interventional, Randomized, Double-blind, Parallel-group, Placebo-controlled Study to Evaluate the Efficacy and Safety of IV Eptinezumab in Adolescents (12-17 Years) for the Preventive Treatment of Chronic Migraine
Acronym: PROSPECT-2
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.