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Inland Northwest Research | Spokane, WA

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A Study of TAK-341 in Treatment of Multiple System Atrophy

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Takeda

Status and phase

Enrolling
Phase 2

Conditions

Multiple System Atrophy

Treatments

Drug: Placebo
Drug: TAK-341

Study type

Interventional

Funder types

Industry

Identifiers

NCT05526391
jRCT2011220029 (Registry Identifier)
2022-000336-28 (EudraCT Number)
TAK-341-2001

Details and patient eligibility

About

The main aim is to see how TAK-341 works after 52 weeks in participants with multiple system atrophy as measured by the Unified Multiple System Atrophy Rating Scale Part I (UMSARS).

The study will enroll approximately 138 patients. Participants will receive a total of 13 intravenous infusions every 4 weeks approximately, these may be either of TAK-341 or placebo, after each infusion some blood samplings will be taken and other assessments completed.

This trial will be conducted in North America, Europe and Asia.

Full description

The drug being tested in this study is called TAK-341. The study will evaluate the efficacy, safety, tolerability, pharmacokinetics (PK), and pharmacodynamics of intravenous (IV) TAK-341 in participants with multiple system atrophy (MSA).

The study will enroll approximately 138 participants. The study comprises a screening period of up to 42 days (6 weeks), a 52-week double-blind treatment period, and a follow-up safety visit. Participants will be randomly assigned (by chance, like flipping a coin) to one of the treatment schedules-which will remain undisclosed to the participant, care provider and investigator during the study:

Early PK Cohort: TAK-341 Early PK Cohort: Placebo Main Cohort: TAK-341 Main Cohort: Placebo

The change from baseline in UMSARS will be measured at Week 52 post-dose.

This multi-center trial will be conducted worldwide. The duration of treatment in this study will be 52 weeks. Participants will make a follow-up visit to the site after approximately 90 days after the last dose of study treatment.

Enrollment

138 estimated patients

Sex

All

Ages

40+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Diagnostic:

  1. The participant has a diagnosis of possible or probable MSA using the modified Gilman et al, 2008 diagnostic criteria.
  2. The participant's onset of first MSA symptoms occurred ≤4 years before screening, as assessed by the investigator.
  3. Evidence of MSA specific symptoms and deficits as measured by the UMSARS scale.

Exclusion criteria

Medical History:

  1. The participant has any contraindication to study procedures.

Diagnostic Assessments:

  1. Presence of confounding diagnosis and/or conditions that could affect participant's safety during the study per investigator judgement.
  2. The participant's participation in a previous study of a disease-modifying therapy (with proven receipt of active treatment) will compromise the interpretability of the data from the present study, per consultation with medical monitor or designee.

Other:

  1. The participant has participated in another study investigating active or passive immunization against α-synuclein (αSYN) for progressive disease (PD) or MSA, or has had immunoglobulin G therapy, within 6 months before screening.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

138 participants in 4 patient groups, including a placebo group

Early PK Cohort: TAK-341
Experimental group
Description:
Participants will be randomized to receive TAK-341 at 4-week intervals for up to 52 weeks.
Treatment:
Drug: TAK-341
Early PK Cohort: Placebo
Placebo Comparator group
Description:
Participants will be randomized to receive placebo at 4-week intervals for up to 52 weeks.
Treatment:
Drug: Placebo
Main Cohort: TAK-341
Experimental group
Description:
Participants will be randomized to receive TAK-341 at 4-week intervals for up to 52 weeks.
Treatment:
Drug: TAK-341
Main Cohort: Placebo
Placebo Comparator group
Description:
Participants will be randomized to receive placebo at 4-week intervals for up to 52 weeks.
Treatment:
Drug: Placebo

Trial contacts and locations

59

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Central trial contact

Takeda Contact

Data sourced from clinicaltrials.gov

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