A Multicentre, Randomised, Double-blind, Placebo-controlled, Parallel-group Trial to Evaluate the Efficacy and Safety of BP1.4979 in Adult Patients With Essential Tremor

Status: Recruiting
Location: See all (14) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

The goal of this clinical trial is to learn if drug BP1.4979 works to treat essential tremors in adults. It will also learn about the safety of drug BP1.4979. The main questions it aims to answer are: * Does the drug BP1.4979 reduce tremors in individuals with essential tremor? * Do participants have a good safety and tolerability of drug BP1.4979? Researchers will compare drug BP1.4979 to a placebo (a look-alike substance that contains no drug) to see if drug BP1.4979 works to treat essential tremors. Participants will: * Take the study drug (active or a placebo) twice daily over a 4-week period * Visit the clinic 5 times for health checkups and questionnaires completion over a period of approximately 7 to 10 weeks * Complete a diary weekly to assess the impact of essential tremor on daily life

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 85
Healthy Volunteers: f
View:

• Male or female ≥18-85 years old

• Confirmed diagnosis of ET, characterized by meeting the following criteria: (a) the presence of a bilateral upper limb action tremor that occurs in isolation; (b) a minimum duration of 3 years; and (c) the tremor may or may not be present in other areas such as the voice, or lower limbs

• ET characterized by a TETRAS-P score of at least 1.5 in either the forward posture, wing beating posture, or finger-to-nose movement of at least one upper extremity

• Female patient: post-menopausal woman having at least 12 months of natural amenorrhea without any alternative medical cause, or woman of childbearing potential using a highly effective method of contraception for the duration of the trial and for 1 month after stopping the investigational medication

Locations
Other Locations
France
CHU Amiens-Picardie
ACTIVE_NOT_RECRUITING
Amiens
CHU Besançon
NOT_YET_RECRUITING
Besançon
Hospices Civils De Lyon Hôpital Neurologique Pierre Wertheimer
RECRUITING
Bron
CHU de Clermont-Ferrand - Hôpital Gabriel Montpied
ACTIVE_NOT_RECRUITING
Clermont-ferrand
CHU Henri Mondor
ACTIVE_NOT_RECRUITING
Créteil
CHU de Lille - Hôpital Roger SALENGRO
ACTIVE_NOT_RECRUITING
Lille
Centre Hospitalier Régional De Marseille - Hôpital de la Timone
ACTIVE_NOT_RECRUITING
Marseille
CHRU Nancy - Hôpital Central
ACTIVE_NOT_RECRUITING
Nancy
CHU de Nice - Hôpital Pasteur 2
ACTIVE_NOT_RECRUITING
Nice
CHU de Nîmes
ACTIVE_NOT_RECRUITING
Nîmes
CHU Poitiers
ACTIVE_NOT_RECRUITING
Poitiers
CHU Rennes - CHU Pontchaillou
ACTIVE_NOT_RECRUITING
Rennes
Hôpitaux Universitaires de Strasbourg - Hôpital de Hautepierre
NOT_YET_RECRUITING
Strasbourg
CHU Purpan - Bâtiment Pierre Paul Riquet
RECRUITING
Toulouse
Contact Information
Primary
Study Medical Director
a.karapet@bioprojet.com
+ 33 6 63 47 43 14
Backup
Clinical Project Manager
s.abid@bioprojet.com
+ 33 1 84 75 34 01
Time Frame
Start Date: 2025-09-17
Estimated Completion Date: 2026-12
Participants
Target number of participants: 50
Treatments
Experimental: BP1.4979
One tablet of BP1.4979 taken twice daily for 4 weeks, approximately 8 to 10 hours apart
Placebo_comparator: Placebo
One tablet of placebo taken twice daily for 4 weeks, approximately 8 to 10 hours apart
Sponsors
Leads: Bioprojet

This content was sourced from clinicaltrials.gov