An Extension Trial to Test if TEV-56286 is Effective in Relieving Multiple System Atrophy
A legfontosabb adatok
- Hol
- Boca Raton, Chicago, Durham, Kansas City, La Jolla, New York, Pittsburgh, Spokane és Tampa (Egyesült Államok)Mind a 10 helyszín megnézése
- Fázis
- 2. fázis
Helyszínek itt: Egyesült Államok
- Boca Raton, FloridaHospital not named in the registryRésztvevőt keres
- Chicago, IllinoisHospital not named in the registryRésztvevőt keres
- Durham, North CarolinaHospital not named in the registryRésztvevőt keres
- Kansas City, KansasHospital not named in the registryRésztvevőt keres
- La Jolla, CaliforniaHospital not named in the registryRésztvevőt keres
- New YorkHospital not named in the registryRésztvevőt keres
- New YorkHospital not named in the registryRésztvevőt keres
- Pittsburgh, PennsylvaniaHospital not named in the registryRésztvevőt keres
- Spokane, WashingtonHospital not named in the registryRésztvevőt keres
- Tampa, FloridaHospital not named in the registryRésztvevőt keres
Kérdések a vizsgálat csapatának
- Milyen gyakran kell bejárnom, és egy-egy alkalom mennyi ideig tart?
- Megtérítik az utazási költséget?
- Megtarthatom a saját orvosomat?
- Mi történik, ha ki akarok lépni?
Contact the study team: see the registry record → Contacts and Locations
Oldal nyomtatása az orvosomnakA vizsgálat adatai
- Ki végzi
- Teva Branded Pharmaceutical Products R&D LLC
- Azonosító
- NCT07197866EU 2025-521642-14-00
- A regiszteradat frissítve
- 2026. október 9.
- Eredeti leírás
The primary objective of the trial is to describe the long-term safety and tolerability of TEV-56286 administered orally for the treatment of adult participants with Multiple System Atrophy (MSA).A teljes eredeti leírásKevesebb
An Open-Label Extension, Multi-Centered, Phase 2 Trial to Describe the Safety and Efficacy of TEV-56286 (Emrusolmin) in Participants With Multiple System Atrophy
The primary objective of the trial is to describe the long-term safety and tolerability of TEV-56286 administered orally for the treatment of adult participants with Multiple System Atrophy (MSA).
A secondary objective of the trial is to further describe the safety and tolerability of TEV-56286.
The planned total duration of the trial is approximately 100 weeks.
Bevonási feltételek: Completion of the treatment period and the week 48(V9) visit of the double-blind trial (TV56286-NDG-20039) whilst remaining compliant with trial requirements; Females of childbearing potential may be included only if they have a negative pregnancy test at the baseline visit; Females of childbearing potential whose male partners are potentially fertile (ie, no vasectomy) must use highly effective birth control methods for the duration of the trial and for 28 days after the last does of IMP; Males who are potentially fertile/reproductively competent (not surgically [eg, vasectomy] or congenitally sterile) and their female partners who are of childbearing potential must use, together with their female partners, highly effective birth control methods for the duration of the trial and for 28 days after the last dose of investigational medicinal product; NOTE - Additional criteria apply, please contact the investigator for more information.
Kizáró feltételek: Is using or consuming any prohibited concomitant medications within the specified exclusionary windows of this trial; Note - Additional criteria apply, please contact the investigator for more information; Is a female participant who is pregnant, plans to become pregnant, or is breastfeeding during the trial; Is of a vulnerable population (eg, people kept in detention or jail).