AB-1005 Delivery for Parkinson's Disease

(PIA Trial)

Not yet recruiting at 3 trial locations
AP
Overseen ByAskFirst Patient Engagement
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)
Prior Safety DataThis treatment has passed at least one previous human trial

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial explores a new method to deliver a medicine called AB-1005 to the brain for treating Parkinson's disease. Researchers aim to determine if this method speeds up and simplifies the delivery process while ensuring the correct amount of medicine reaches the brain. The study also tests the safety of this method for up to six months post-procedure. The trial seeks participants who have had Parkinson's for over 10 years and experience symptoms such as slow movement, muscle stiffness, or tremors. As a Phase 2 trial, the research focuses on measuring the treatment's effectiveness in an initial, smaller group of people.

What prior data suggests that this new delivery method is safe for delivering AB-1005?

Research has shown that AB-1005 is generally well-tolerated by people with Parkinson's disease. In an earlier study, researchers administered a single dose of AB-1005 directly into the putamen, a part of the brain, and reported no serious side effects. This suggests the treatment is safe, with no major harmful effects linked to the gene therapy itself.

Another study confirmed that AB-1005 is safe and well-tolerated, as participants experienced no major side effects. These findings offer a positive outlook on the safety of AB-1005 for those considering participation in a clinical trial.12345

Why are researchers excited about this trial?

Researchers are excited about AB-1005 for Parkinson's Disease because it introduces a novel delivery method called convection-enhanced delivery (CED) combined with real-time imaging using iMRI. Unlike traditional treatments that primarily involve oral medications or deep brain stimulation, CED allows for direct delivery of the drug into the brain, potentially increasing precision and effectiveness. This method may improve targeting of the affected brain regions and minimize side effects, offering a promising alternative to existing therapies.

What evidence suggests that this new delivery method for AB-1005 is effective for Parkinson's Disease?

Studies have shown that AB-1005, an experimental gene therapy, can help improve movement problems in people with Parkinson's disease. In an 18-month study, patients experienced about 2.2 more hours each day of well-controlled symptoms, known as "Good ON" time. The therapy proved generally safe, with no serious side effects directly linked to it. Further research indicated that most patients maintained stable results over time and required less additional medication. This suggests that AB-1005 might help reduce movement issues related to Parkinson's disease. Participants in this trial will receive AB-1005 through a prescriptive infusion algorithm for standardized intraputaminal administration, monitored under iMRI.45678

Are You a Good Fit for This Trial?

This trial is for people aged 45–75 who have had Parkinson's disease for over 10 years, with significant movement problems like tremor, rigidity, and balance issues. Participants must be on stable medication and agree to use birth control after the procedure.

Inclusion Criteria

I am between 45 and 75 years old.
My Parkinson's disease is at stage III or IV when not taking medication.
Female participants cannot be pregnant or breastfeeding at screening; WOCBP must have a negative highly sensitive pregnancy test at required assessments
See 9 more

Exclusion Criteria

Presence or history of psychosis or impulse control disorder as determined by neurologist
I have not had unstable angina or a heart attack in the past year.
Clinically significant cognitive impairment with MoCA score less than 25
See 22 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Technical Stage 0

Test if the new delivery method can consistently deliver AB-1005 to the putamen using MRI monitoring

1-2 weeks

Technical Stage 1

Evaluate the suitability of PIA-based infusion for standardized intraputaminal administration of AB-1005 via CED under iMRI monitoring

1-2 weeks

Technical Stage 2

Confirm the new delivery method works without brain imaging by MRI, using standard operating room tools including brain imaging by CT

1-2 weeks

Safety Assessment

Assess the safety and tolerability of the new delivery method for AB-1005 up to 6 months after surgery

6 months

Follow-up

Participants are monitored for safety and effectiveness after treatment

6 months

Long-term Follow-up

Participants' health will be monitored for up to 10 years after their surgery

10 years

What Are the Treatments Tested in This Trial?

Interventions

  • AB-1005
  • Prescriptive Infusion Algorithm

Trial Overview

The study tests a new surgical method (Prescriptive Infusion Algorithm) to deliver AB-1005 directly into the brain area affected by Parkinson's using imaging guidance. The goal is to see if this approach is safe and effective.

How Is the Trial Designed?

1

Treatment groups

Experimental Treatment

Group I: Stage 1Experimental Treatment2 Interventions

Find a Clinic Near You

Who Is Running the Clinical Trial?

AskBio Inc

Lead Sponsor

Trials
8
Recruited
440+

Bayer

Industry Sponsor

Trials
2,291
Recruited
25,560,000+
Founded
1863
Headquarters
Leverkusen, Germany
Known For
Pharmaceutical Innovations
Top Products
Aspirin, Aleve, Yaz, Nexavar

Bill Anderson

Bayer

Chief Executive Officer since 2023

BSc in Chemical Engineering from the University of Texas, MSc in Chemical Engineering and Management from MIT

Michael Devoy profile image

Michael Devoy

Bayer

Chief Medical Officer since 2014

MD, PhD

Citations

AskBio presents 18-month Phase Ib trial results of AB-1005 ...

Motor Diaries for the Moderate Cohort reported a 2.2-hour improvement in “Good ON” state time, which was clinically meaningful; a 0.5-hour ...

AskBio Announces Publication of Complete Results ...

AB-1005 was well tolerated with no attributed serious adverse events in participants with mild or moderate Parkinson's disease (PD) through 18 months post-gene ...

Overviewing 36-Month, Phase 1b Data Testing Gene ...

Among 6 patients with mild PD and 5 patients with moderate PD, findings showed that most mild participants had stable outcomes on the Movement ...

NCT07081841 | AB-1005 Long-Term Follow-up Study

This is an observational study in which safety laboratories and non-invasive routine clinical assessments are conducted to gauge long term safety and efficacy.

Investigational Gene Therapies for Parkinson's Disease - PMC

Results at 6 months showed significant motor improvement and reduction of levodopa dose, and a 56% increase in PET signal using 6-[18F]fluoro-l- ...

AskBio's AB-1005 and AB-1002 Receive Pioneering ...

AskBio receives FDA Fast Track and MHRA Innovation Passport designations for AB-1005 investigational GDNF gene therapy for Parkinson's disease.

First European Participants Randomized in AskBio Phase ...

AB-1005 is an investigational gene therapy that has not been approved by any regulatory authority, and its efficacy and safety have not been ...

Phase 1b Safety and Preliminary Efficacy of Bilateral ...

These preliminary findings suggest AAV2-GDNF is well tolerated in participants with PD, demonstrating general stability of the Mild Cohort and possible ...