A Study to Evaluate in Patients With Parkinsonian Type Disorders

Idiopathic Parkinson Disease Clinical Trial

Official title:

A Phase 2 Study to Evaluate the Safety, Tolerability and Initial Efficacy of Pramipexole ER, Given With Aprepitant in Patients With Idiopathic Parkinson's Disease

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT03683225
• Other study ID #: CTC-002
• Status: Active, not recruiting
• Phase: Phase 2
• Start date: April 1, 2019
• Est. completion date: December 30, 2024

Study information

• Verified date: October 2023
• Source: Chase Therapeutics Corporation
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

A Phase 2 study to evaluate the safety, tolerability and initial efficacy of pramipexole ER, given with aprepitant in patients with parkinsonian type disorders

Description:

Methodology:

This is an initial Phase 2, rising-dose, single-blind, out-patient, sequential-treatment study in up to 24 patients with idiopathic Parkinson's disease of about 5 months duration. All participants will have idiopathic Parkinson's disease (PD).

Subjects will sign a consent form prior to any study related procedure and will complete baseline screening assessments.

The study will be conducted in three parts:

Part 1: All eligible patients switch from their dopaminergic treatment to the equivalent dose of pramipexole ER in the judgement of the investigator. Then, pramipexole ER is titrated alone up to the patients' optimal dose or to the protocol maximum allowed dose for Part 1 of 4.5 mg/day.

Part 2: Add-on aprepitant and continue the titration of pramipexole ER from the optimal dose (or 4.5 mg/day) determined in Part 1 to the optimal dose not to exceed the protocol limit of 9.0mg/day, given in combination with aprepitant.

Part 3: Maintain the dose of pramipexole ER found in Part 2 given in combination with aprepitant for 3 months with periodic safety and efficacy checks.

During Parts 1 and 2, subjects will be evaluated at in-clinic visits for safety and tolerability at intervals not to exceed once weekly ± 2 days and additionally by telephone or in-clinic visits, as considered clinically appropriate, at each dose change.

During Part 3, this optimal pramipexole ER/aprepitant regimen will be stably maintained for 3 months in association with monthly in-clinic laboratory and clinical evaluations. Safety and tolerability will continue to be evaluated by telephone or in-clinic visits, as deemed clinically appropriate.

Pramipexole ER tablets will be administered with or without aprepitant, orally once daily in the morning. Subjects will take 1-3 pramipexole ER tablets daily.

Aprepitant will be administered orally in a fixed daily dose by means of a single capsule containing 80 mg.

At study completion (or at other times in accordance with Stopping Rules given below), study medications will be discontinued, and participants will be returned to their pre-admission therapeutic regimen as considered medically appropriate. Investigators will always have the option of making necessary and appropriate changes to protocol dose optimization schedules in consultation with the Sponsor.

An independent DSMB will be appointed to have responsibility for safeguarding the interests of the trial subjects and assessing the safety and tolerability of the study treatments during the trial. The DSMB will meet when 10 patients complete the study and when all patients complete the study.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 24
• Est. completion date: December 30, 2024
• Est. primary completion date: December 30, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 40 Years to 80 Years

Eligibility

Inclusion Criteria:

1. Patient must have signed an Institutional Review Board (IRB) approved informed consent document indicating that they understand the purpose of and procedures required by the study and are willing to participate in the study and comply with all study procedures and restrictions. Informed consent must be obtained from the patient and/or a designated representative prior to initiating screening procedures to evaluate eligibility of the study.

2. Males and females aged 40 - 80 years inclusive.

3. Meet criteria for the diagnosis of possible/ probable idiopathic Parkinson's disease (PD; Postuma RB, et al. 2015)

4. Have not previously been treated with CD/LD.

5. PD severity in the Hoehn & Yahr 2 to 3 range.

Exclusion Criteria:

1. Women who are pregnant or may become pregnant.

2. Nursing mothers.

3. Individuals who have taken a study medication (pramipexole and/or aprepitant) within 3 months of study admission.

4. Moderate and severe renal impairment (Creatinine Clearance: < 60 mL/min calculated by Cockcroft and Gault equation)

5. Severe hepatic impairment (Child-Pugh C)

6. Hypersensitivity to any component of either study medication

7. Being treated with the following medications:

• Pramipexole

• Centrally acting dopamine antagonists during preceding month

• Pimozide

• Strong CYP3A4 inducer or inhibitor

• Warfarin (a CYP2C9 substrate)

• Hormonal contraceptives

8. Patients considered unlikely to co-operate in the study, and/or poor compliance anticipated by the investigator.

9. Patients who have any clinically significant hypotension or ECG abnormality.

10. Any other clinically relevant acute or chronic diseases which could interfere with patients' safety during the trial, or expose them to undue risk, or which could interfere with study objectives.

11. Patients who have participated in another clinical trial with an investigational drug within previous 30 days.

Related Conditions & MeSH terms

• Idiopathic Parkinson Disease
• Parkinson Disease

Intervention

Combination Product:
• CTC-413
pramipexole ER, given with aprepitant

Locations

Country	Name	City	State
United States	Quest Research	Farmington Hills	Michigan

Sponsors (1)

Lead Sponsor	Collaborator
Chase Therapeutics Corporation

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of participants with adverse events -Safety by Incidence of Treatment-Emergent Adverse Events	Number of participants with treatment-related adverse events as assessed by CTCAE v4.0" . Incidence and nature of adverse events; vital signs;	multiple times for the duration of the study (baseline through Month 3)
Primary	Number of participants with change in weight	Number of participants with a change in weight (either by pounds or kilograms) from baseline	mulitple times from baseline through Month 3
Primary	Number of participants with change in in physical examine	physical examination changes General appearance,Head, eyes, ears, nose, and throat, Respiratory, Cardiovascular, Musculoskeletal, Abdomen, Neurologic, Extremities, Dermatologic, Lymphatic)	multiple times for the duration of the study (baseline through Month 3)
Primary	Number of participants with change in in clinical laboratory evaluations	changes in clinical laboratory evaluations (Creatinine, Potassium(K+),Sodium (Na+) , Chloride (Cl-), Magnesium (Mg++), Calcium, Inorganic phosphate, Glucose, Urea,Bilirubin (Total) ,Bilirubin (direct), AST, ALT, GGT, Alkaline phosphatase, Total Protein Albumin,	multiple times for the duration of the study (baseline through Month 3)
Primary	Number of participants with change in Electrocardiography (ECG)	ECG (standard digital 12-lead in singlicate).	multiple times for the duration of the study (baseline through Month 3)
Secondary	Unified Parkinson's Disease Rating Scale (MDS-UPDRS)	Change from baseline in the MDS-UPDRS Part 4 for motor fluctuations and dyskinesia severity will be assessed hourly x3 on assessment days.motor complications (six items). Subscale has 0-4 ratings, where 0 = normal, 1 = slight, 2 = mild, 3 = moderate, and 4 = severe. Total score 0-24.	multiple times from baseline through Month 3
Secondary	modified Columbia-Suicide Severity Rating Scale	3 question scale to to gage is the subject is having suicidal tendencies. If the response is "YES" to Question 1 or 2, or if the response to Question 3 reveals a concern about a significant level of suicidality, the subject would undergo a more detailed assessment by a qualified clinician who has experience in the evaluation of suicidal ideation and behavior, either at the site or by referral to an outside clinician. In either case, appropriate documentation of the clinical issues and management plan will be required in a narrative that would be placed in the subject's study record. Questions are 'yes' or 'no'	multiple times from baseline through Month 3
Secondary	Pharmacokinetics of pramipexole and aprepitant	Plasma concentrations of pramipexole and aprepitant will be measured	multiple times from baseline through Month 3