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Completed

NCT Number: NCT00919555

Combination Therapy in Amyotrophic Lateral Sclerosis (ALS)

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.

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Key information

Age range

18 year–85 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1 / Phase 2

Primary location

Phoenix Neurological Associates, LTD

Phoenix, Arizona, 85018, United States

About this study

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

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Pioglitazone and Tretinoin

Drug

Tretinoin: 1 pill twice a day (10 mg/bid) Pioglitazone HCL: 1 pill once a day (30 mg/qd)

Tretinoin and Pioglitazone HCL

Drug

Tretinoin 10 mg 1 pill po twice a day Pioglitazone HCL 30 mg 1 pill po once a day

Placebo

Drug

Placebo

Primary outcomes

  1. To evaluate the safety and efficacy of Tretinoin and Pioglitazone HCL in patients with ALS

    Time frame: 3 years

Secondary outcomes

  1. 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

Sponsors and collaborators

Lead sponsor

Phoenix Neurological Associates, LTD

Other

Registry information

Official study title

Phase IIA Trial: Tretinoin and Pioglitazone HCL Combination Therapy in Amyotrophic Lateral Sclerosis

Acronym: PNA

Important dates

Study start
2008
Primary completion
2009
Study completion
2012
First posted
Jun 12, 2009
Registry last updated
Nov 30, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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