Study of the Safety and Efficacy of Tropicamide Thin Films to Reduce Hypersalivation in Parkinson's Patients

Sponsor

NeuroHealing Pharmaceuticals Inc. (Industry)

Overall Status

Completed

CT.gov ID

NCT01844648

Collaborator

Michael J. Fox Foundation for Parkinson's Research (Other)

Enrollment

Locations

Arms

Duration (Months)

Patients Per Site

0.3

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

To study the safety and efficacy of tropicamide 1 mg intra-oral slow dissolving muco-adhesive thin films compared to placebo to reduce hypersalivation in PD patients manifesting sialorrhea complaints.

Condition or Disease	Intervention/Treatment	Phase
Sialorrhea (Excessive Drooling)	Drug: NH004 tropicamide Drug: NH004 Placebo	Phase 2

Detailed Description

This is a double-blind, placebo-controlled, randomized, crossover, multicentre study comparing intra-oral slow dissolving muco-adhesive thin films containing tropicamide 1 mg or Placebo. Patients will receive each treatment twice daily (1 h after breakfast and 1 h after lunch) for 1-week.

Patients will be evaluated for eligibility during the 14-day screening period. Those patients meeting all entry criteria at baseline will be randomized (1:1) to receive first tropicamide followed by placebo films or vice versa. Patients will return for regularly scheduled visits at Weeks 1 and 3 or at early discontinuation.

Study Design

Study Type:

Interventional

Actual Enrollment :

30 participants

Allocation:

Randomized

Intervention Model:

Crossover Assignment

Masking:

Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

Primary Purpose:

Treatment

Official Title:

A Randomized, Double-blind, Placebo-controlled, Crossover Study of the Safety and Efficacy of Tropicamide 1 mg Intra-oral Slow Dissolving Muco-adhesive Thin Films to Reduce Hypersalivation in PD Patients Manifesting Sialorrhea Complaints

Study Start Date :

Apr 1, 2013

Actual Primary Completion Date :

Oct 1, 2015

Actual Study Completion Date :

Dec 1, 2015

Arms and Interventions

Arm	Intervention/Treatment
Experimental: NH004 tropicamide tropicamide 1 mg thin film, twice daily for 7 days	Drug: NH004 tropicamide Intra-oral slow dissolving muco-adhesive thin film containing 1 mg tropicamide
Placebo Comparator: NH004 placebo placebo thin film, twice daily for 7 days	Drug: NH004 Placebo Intra-oral slow dissolving muco-adhesive thin film

Arm

Intervention/Treatment

Experimental: NH004 tropicamide

tropicamide 1 mg thin film, twice daily for 7 days

Drug: NH004 tropicamide

Intra-oral slow dissolving muco-adhesive thin film containing 1 mg tropicamide

Placebo Comparator: NH004 placebo

placebo thin film, twice daily for 7 days

Drug: NH004 Placebo

Intra-oral slow dissolving muco-adhesive thin film

Outcome Measures

Primary Outcome Measures

modified Teachers Drooling Scale (% responding) [one week]
The primary endpoint for this trial is the difference in responder rate between tropicamide and placebo. Responders will be defined as subjects whose mean sialorrhea score improved by at least 30% as compared to baseline in the 9-point modified Teachers Drooling Scale (mTDS).

Secondary Outcome Measures

modified Teachers Drooling Scale (mean) [one week]
Difference in the mean sialorrhea scores between placebo and tropicamide in the 9-point modified Teachers Drooling Scale (mTDS).
Sialorrhea Clinical Scale for Parkinson's Disease (mean) [one week]
- Difference in the mean sialorrhea scores between placebo and tropicamide in the Sialorrhea Clinical Scale for Parkinson's Disease (SCS-PD).
UPDRS Part II sialorrhea item (mean) [one week]
Difference in the mean sialorrhea scores between placebo and tropicamide in the UPDRS Part II sialorrhea item (#6).
Visual Analg Scale [one week]
Saliva buccal content as measured by a Visual Analog Scale (VAS) score, evaluated before and during 3 hours after treatments administration.

Eligibility Criteria

Criteria

Ages Eligible for Study:

30 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion criteria:

Patients with idiopathic Parkinson's disease, according to the UK Brain Bank criteria.
Patients complaining of drooling, with a score of at least 6 points in the SCS-PD scale.
Patients above 30 years old.
Patients with Hoehn & Yahr score between I-IV.
Male or non-pregnant female. Females of child-bearing potential will be required to have undergone a pregnancy test with negative results prior to entry to the study and agree to use contraceptive measures for the duration of the study.
Patients must have used the same antiparkinsonian medications and at the same dose for the last month. No changes in the medication for PD are expected during the study.

Exclusion criteria:

Pregnant women.
Patients with a secondary parkinsonian syndrome, parkinsonism-plus syndromes, heredodegenerative disorders or benign parkinsonism.
Patients with a diagnosis of major depression or psychosis according to the DSM-IV.
Patients with MMSE score equal to or lower than 24.
Patients with a current diagnosis of substance abuse (DSM-IV) or history of alcohol or drug abuse in the past 3 months.
Patients with hallucinations.
Patients with a current clinically significant gastrointestinal, renal, hepatic, endocrine, pulmonary or cardiovascular disease, including hypertension that is not well-controlled, asthma, chronic obstructive pulmonary disease (COPD) and Type I diabetes.
Patients with a second- or third-degree atrioventricular block or sick sinus syndrome, uncontrolled atrial fibrillation, severe or unstable angina, congestive heart failure, myocardial infarction within 3 months of the screening visit, or significant ECG abnormality, including QTc ≥ 450 msec (males) or ≥ 470 msec (females), where QTc is based on Bazett's correction method.
Patient with a neoplastic disorder, which is either currently active or has been in remission for less than one year.
Patients with a history or a current diagnosis of HIV, or tests positive for Hepatitis B or C antibodies, or Hepatitis B surface antigen
Patients who have participated in a previous clinical trial within 30 days of entry into the study (screening visit) or have received treatment with any investigational compound within 30 days.
Patients with hypersensitivity to atropine or other anticholinergic drugs.
Patients who have experienced adverse effects as a result of taking anticholinergic drugs.
Patients who are receiving any anticholinergic drug or an anticholinesterase agent.
Patients who started or changed the dose of any of the following medications in the previous week: tricyclic antidepressants, monoamine oxidase-A inhibitors, antipsychotics, benzodiazepines, opioids, antihistamines, carbamazepine, NSAIDs.
Patients with significant dental/oral pathology.
Patient with any abnormality that the investigator deems to be clinically relevant, either on medical history, physical examination, ECG or in a diagnostic laboratory test.
Patients with closed-angle Glaucoma or those at high risk of suffering it after treatment with anticholinergic agents.
Patients with Prostatic Adenoma.
In the judgment of the Clinical Investigator, the patient is likely to be non-compliant or uncooperative during the study.

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Hôpital de la Salpêtrière	Paris	Cedrex 13	France	75651
2	Hôpital Paul de Viguier	Toulouse	Cedrex 9	France	31059
3	Hôpital Haut Lévêque	Bordeaux	Pessac	France	33604