Combination Therapy in Amyotrophic Lateral Sclerosis (ALS) (PNA)

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Phoenix Neurological Associates, LTD
ClinicalTrials.gov Identifier:
NCT00919555
First received: June 8, 2009
Last updated: November 29, 2012
Last verified: November 2012

June 8, 2009
November 29, 2012
June 2008
November 2009   (final data collection date for primary outcome measure)
To evaluate the safety and efficacy of Tretinoin and Pioglitazone HCL in patients with ALS [ Time Frame: 3 years ] [ Designated as safety issue: Yes ]
Same as current
Complete list of historical versions of study NCT00919555 on ClinicalTrials.gov Archive Site
To determine if cerebrospinal fluid tau levels decline over the course of treatment and if the level of tau decline correlates with response in treatment measured by ALSFRS [ Time Frame: 3 years ] [ Designated as safety issue: No ]
Same as current
Not Provided
Not Provided
 
Combination Therapy in Amyotrophic Lateral Sclerosis (ALS)
Phase IIA Trial: Tretinoin and Pioglitazone HCL Combination Therapy in Amyotrophic Lateral Sclerosis

The purpose of the study is to determine the safety and the efficacy of Tretinoin and Pioglitazone HCL in patients with ALS who are currently on Riluzole.

Physicians at Phoenix Neurological Associates (PNA) are looking for individuals diagnosed with ALS to participate in a double-blind, placebo controlled study of Tretinoin and Pioglitazone HCL, used in combination with Riluzole, for treating ALS. This investigator initiated trial conducted by Dr. Todd Levine and Dr. David Saperstein will help determine whether Tretinoin and Pioglitazone HCL, in combination, can slow the progression of ALS.

At present, there is little to no effective therapy for ALS, nor is there a known cause. Therefore there is a tremendous unmet need for more effective therapy for this disease and that is why the physicians at PNA have been very interested in the role of developing a more active anti-excitotoxic cocktail for patients with ALS. Since recent data have suggested that inflammatory mechanisms may interact with and promote neurodegeneration (where cells in the spinal cord and brain are lost), there have been a number of anti-inflammatory treatment strategies that have been evaluated in animal models. Some studies have shown that mice that were given Pioglitazone HCL demonstrated improved muscle strength and body weight, exhibited a delayed disease onset as well as had a longer survival rate compared to non treated mice.

In addition to these studies, retinoic acids have been studied extensively in various models of the injured nervous system. These studies have shown that retinoic acids, such as Tretinoin may be neuroprotective and support axonal growth, which could in turn slow disease progression.

The purpose of this study is to determine if such a drug "cocktail" could offer the best chance of attaining a significant reduction in disease progression by utilizing currently available FDA-approved agents

Interventional
Phase 1
Phase 2
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Caregiver, Investigator)
Primary Purpose: Treatment
Amyotrophic Lateral Sclerosis
  • Drug: Pioglitazone and Tretinoin
    Tretinoin: 1 pill twice a day (10 mg/bid) Pioglitazone HCL: 1 pill once a day (30 mg/qd)
  • Drug: Tretinoin and Pioglitazone HCL
    Tretinoin 10 mg 1 pill po twice a day Pioglitazone HCL 30 mg 1 pill po once a day
  • Drug: Placebo
    Placebo
  • Active Comparator: Tretionoin and Pioglitazone HCL
    20 patients will be randomized blindedly to Tretinoin and Pioglitazone HCL
    Interventions:
    • Drug: Pioglitazone and Tretinoin
    • Drug: Tretinoin and Pioglitazone HCL
  • Placebo Comparator: Sugar Pill
    10 Patients will randomly receive placebo
    Intervention: Drug: Placebo
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
28
March 2012
November 2009   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • El Escorial Classification of laboratory supported probable, probable, or definite ALS
  • Age 18 - 85 years
  • Male or female
  • FVC greater than or equal to 70% predicted

Exclusion Criteria:

  • Patients with FVC below 1.5 L or below 70% predicted
  • History of liver disease
  • Severe renal failure (CrCl<30)
  • History of coronary artery disease requiring placement of stents, bypass surgery or previous myocardial infarction
  • EKG at baseline with evidence for previous myocardial infarction, cardiomyopathy, or arrhythmia
  • History of intolerance to Riluzole, Tretinoin, or Pioglitazone HCL
  • History of diabetes
  • Any other comorbid condition which would make completion of trial unlikely
Both
18 Years to 85 Years
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00919555
20071808
Yes
Phoenix Neurological Associates, LTD
Phoenix Neurological Associates, LTD
Not Provided
Principal Investigator: Todd D Levine, MD Phoenix Neurological Associates, LTD
Phoenix Neurological Associates, LTD
November 2012

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP