A Study of KPS-0373 in Patients With Spinocerebellar Degeneration (SCD)

Kissei

Status and phase: Completed; Phase 2

Conditions: Spinocerebellar Degeneration

Treatments: Drug: Placebo; Drug: KPS-0373

Study type: Interventional

Funder types: Industry

Identifiers

NCT01004016

KPS1202

Details and patient eligibility

About

To evaluate the efficacy and safety of KPS-0373 in patients with SCD.

Enrollment: 20 estimated patients

Sex: All

Ages: 20+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Japanese SCD patients with mild to moderate ataxia

Exclusion criteria

• Patients with secondary ataxia
• Patients with clinically significant hepatic, renal, or cardiovascular dysfunction

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Crossover Assignment

Masking: Double Blind

---

20 participants in 2 patient groups, including a placebo group

Placebo

Placebo Comparator group

Treatment:

Drug: Placebo

KPS-0373

Experimental group

Treatment:

Drug: KPS-0373