BEN-2001 in Parkinson Disease Patients With Excessive Daytime Sleepiness (CASPAR)

B

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Status and phase

Completed
Phase 2

Conditions

Parkinson Disease
Excessive Daytime Sleepiness

Treatments

Drug: Placebo
Drug: BEN-2001

Study type

Interventional

Funder types

Industry

Identifiers

NCT03194217
BB-2001-201b

Details and patient eligibility

About

This phase 2b study is designed as multicentre, multinational, randomized, double blind, parallel group and placebo controlled with three doses of Bavisant (0.5, 1, and 3 mg/d) in subjects with excessive daytime sleepiness with Parkinson's disease.

Full description

Phase 2b study will be conducted with the aim of investigating the efficacy and safety of three fixed doses of Bavisant (0.5, 1 and 3 mg/d) compared to placebo for the treatment of excessive daytime sleepiness (EDS) in subjects with Parkinson's disease.

Enrollment

244 patients

Sex

All

Ages

50 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Subjects of either sex aged 50 to 80 years *Subjects with previous diagnosis of Parkinson's disease (following the UK Parkinson's disease society brain bank clinical diagnostic criteria)*
  • Subjects capable of understanding and complying with protocol requirements
  • Subjects with medical history of excessive daytime sleepiness

Exclusion criteria

  • Subjects with excessive daytime sleepiness due to conditions other than Parkinson's disease (including narcolepsy)
  • Subjects with clinical evidence of depression with significant psychiatric comorbidities (Hamilton Rating Scale for Depression - HAM-D score greater than or equal to 17; with or without treatment)
  • Subjects with evidence of significant fatigue (Fatigue Severity Scale - FSS greater than or equal to 36
  • Subjects with known history of abuse of alcohol or other addictive substances in the 6 months prior to inclusion.
  • Subjects with known allergies or hypersensitivity to Bavisant or any of its excipients.
  • Subjects who are pregnant or lactating.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

244 participants in 4 patient groups, including a placebo group

BEN-2001, 0.5mg
Experimental group
Description:
Experimental treatment
Treatment:
Drug: BEN-2001
Placebo
Placebo Comparator group
Description:
Placebo comparator
Treatment:
Drug: Placebo
BEN-2001, 1.0mg
Experimental group
Description:
Experimental treatment
Treatment:
Drug: BEN-2001
BEN-2001, 3.0mg
Experimental group
Description:
Experimental treatment
Treatment:
Drug: BEN-2001

Trial documents
2

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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