RT001 in Patients With Progressive Supranuclear Palsy (PSP) PROGRESSIVE SUPRANUCLEAR PALSY

NCT ID: NCT04937530

Last Updated: 2021-06-25

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE2
• Total Enrollment: 40 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-06-23
• Study Completion Date: 2022-08-30

Brief Summary

This is a randomized, placebo-controlled trial of RT001 in patients with PSP.

Detailed Description

This is a randomized, placebo-controlled trial of RT001 in patients with PSP to assess the efficacy, safety and tolerability of RT001. Subjects will be randomized to RT001 or placebo and will receive study drug for 48 weeks.

Conditions

Progressive Supranuclear Palsy

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

RT001

RT001 960 mg capsule. 3 capsules TID for 4 weeks, followed by 3 capsules BID for the remaining 44 weeks.

Group Type: EXPERIMENTAL

RT001

Intervention Type: DRUG

RT001 8.64 g/d (3 capsules TID) for 1 month followed by 5.76 g/d (3 capsules BID) for an additional 11 months

Placebo

Inactive comparator capsule 960 mg (safflower oil). 3 capsules TID for 4 weeks, followed by 3 capsules BID for the remaining 44 weeks.

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

Placebo Comparator: Placebo Inactive comparator capsule 960 mg/capsule: 3 capsules TID for 4 weeks, followed by 3 capsules BID for the remaining 44 weeks.

Interventions

RT001

RT001 8.64 g/d (3 capsules TID) for 1 month followed by 5.76 g/d (3 capsules BID) for an additional 11 months

Intervention Type: DRUG

Placebo

Placebo Comparator: Placebo Inactive comparator capsule 960 mg/capsule: 3 capsules TID for 4 weeks, followed by 3 capsules BID for the remaining 44 weeks.

Intervention Type: DRUG

Other Intervention Names

di-deuterated linoleic acid ester; safflower oil

Eligibility Criteria

Inclusion Criteria

1. Sign the informed consent form prior to entry into the study

2. Male or female subject with age 40 years to 80 years at the time of signed consent

3. Meets the MDS-PSP study group criteria for possible or probable progressive supranuclear palsy with Richardson syndrome (postural instability and falls with vertical ocular motor dysfunction)

4. Presence of PSP symptoms for less than 4 years

5. Score of <40 on the PSPRS-28

6. Ambulatory patients (with or without assistive device - no handheld help) and capable of performing study assessments/evaluations

7. Subject has an identified, reliable, study partner (e.g., caregiver, family member, social worker, or friend) who can assist in assuring that the subject is able to travel to the required visits.

8. Willing to provide the necessary blood samples

Exclusion Criteria

1. Received treatment with other experimental therapies within the last 30 days prior to the first dose. The last dose of the prior experimental agent must have occurred more than 5 half-lives prior to enrollment in the current trial.

2. Previously received treatment with RT001

3. Refusal to discontinue fish oils or other oil-based supplements for the duration of the study (Screening/Baseline till last study procedure completed)

4. Mini mental state examination (MMSE) score less than 20 at screening

5. Subject resides at a skilled nursing or dementia care facility, or admission to such a facility is planned during the study period

6. Evidence of any clinically significant neurological disorder other than PSP in particular CBS

7. Evidence of a clear and robust benefit from levodopa at the time of screening. Participants are permitted to take levodopa and other Parkinson's medications if the dose had been stable for 60 days prior to screening

8. The subject has a history of or currently has schizophrenia, schizoaffective disorder or bipolar disorder according to DSM-V or ICD-10 criteria

9. Subject has had a significant illness or infection requiring medical intervention in the past 30 days

10. Subject has evidence of any disease or condition (based on either history, physical or laboratory values) that might interfere with the conduct of the study

11. Is currently receiving active deep brain stimulation (DBS) that cannot be turned off

12. Any condition with a life expectancy of less than 2 years

13. Female who is breastfeeding or has a positive pregnancy test

14. Male participant or female participant of childbearing potential, who is sexually active and unwilling/unable to use a highly effective birth control method throughout the study

15. Unwilling or unable to comply with the requirements of this protocol, including the presence of any condition (physical, mental, or social) that is likely to affect the subject's ability to return for visits as scheduled

16. History, within the last 2 years, of alcohol abuse or physical opioid dependence

• Minimum Eligible Age: 40 Years
• Maximum Eligible Age: 80 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Biojiva LLC

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Stefan Lorenzl, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Ludwig-Maximilians - University of Munich

Locations

Agaharied Teaching Hospital, University of Munich

Munich, MD, Germany

Site Status: RECRUITING

Countries

Germany

Central Contacts

Mark G. Midei, MD

Role: CONTACT

mark@retrotope.com

(650) 437-0700

Facility Contacts

Mark G. Midei, MD

Role: primary

mark@retrotope.com

Other Identifiers

RT001-013

Identifier Type: -

Identifier Source: org_study_id