Study of NGX267 Oral Capsules in Patients With Xerostomia Associated With Sjorgren's Syndrome
This study has been completed.
Sponsor:
TorreyPines Therapeutics
Information provided by:
TorreyPines Therapeutics
ClinicalTrials.gov Identifier:
NCT00637793
First received: March 11, 2008
Last updated: January 28, 2009
Last verified: January 2009
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Purpose
The purpose of this study is to evaluate the effectiveness of NGX267 in the improvement of decreased salivary flow associated with primary or secondary Sjögren's syndrome.
For each patient, the study includes four periods of treatment separated by a washout period that may range from 4 - 8 days according to patient and site discretion. Each treatment period includes two overnight stays in the clinic. One dose of study drug is taken during each treatment period
| Condition | Intervention | Phase |
|---|---|---|
|
Xerostomia Sjogren's Syndrome |
Drug: NGX267 |
Phase 2 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Crossover Assignment Masking: Double-Blind Primary Purpose: Treatment |
| Official Title: | A Double-Blind, Placebo-Controlled, Cross Over Study Using a Latin Square Design to Evaluate the Safety, Tolerability, and Efficacy of NGX267 Oral Capsules in Patients With Xerostomia Associated With Sjogren's Syndrome |
Resource links provided by NLM:
Further study details as provided by TorreyPines Therapeutics:
Primary Outcome Measures:
- Quantitative and qualitative assessment of dry mouth [ Time Frame: 36 days ] [ Designated as safety issue: No ]
Secondary Outcome Measures:
- Tolerability and safety of NGX267 [ Time Frame: 36 days ] [ Designated as safety issue: Yes ]
| Estimated Enrollment: | 24 |
| Study Start Date: | February 2008 |
| Study Completion Date: | November 2008 |
| Arms | Assigned Interventions |
|---|---|
|
Placebo Comparator: 1
Placebo capsules
|
Drug: NGX267
2 capsules in the am of each treatment period
|
|
Experimental: 2
2 capsules in the am of each treatment period
|
Drug: NGX267
2 capsules in the am of each treatment period
|
|
Experimental: 3
2 capsules in the am of each treatment period
|
Drug: NGX267
2 capsules in the am of each treatment period
|
|
Experimental: 4
2 capsules in am of each treatment period
|
Drug: NGX267
2 capsules in the am of each treatment period
|
Eligibility| Ages Eligible for Study: | 21 Years to 55 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Males and females aged 21 to 55 years, diagnosed with primary or secondary Sjögren's syndrome.
- Patients with a complaint of dry mouth based upon difficulty in speaking, swallowing, a sensation of mouth or throat dryness, lip or tongue dryness, or a level of thirst of sufficient intensity for the patient to seek therapy.
- Females of childbearing potential must not be at risk for pregnancy during the study. Females not of childbearing potential include postmenopausal and women who have been surgically sterilized.
- Patients must not be in an acute phase of illness.
Exclusion Criteria:
- Patients who have clinically significant reduction kidney function. cardiovascular abnormalities; lymphoma secondary to Sjögren's syndrome; pulmonary disease; the presence of enlarged salivary glands; physical closure of the salivary gland or known surgical procedure on the lacrimal punctum.
- Patients with diagnoses of a current gastrointestinal (GI) disease that would be exacerbated by the use of cholinomimetics; a current and acute psychiatric disorder, acute iritis, narrow angle glaucoma, or retinal disease as determined by medical history and physical examination.
- Patients who are otherwise judged inappropriate for inclusion in the study by the investigator
- Patients who have received any experimental drugs or devices or participated in any clinical trial within 30 days prior to screening including participation in a previous NGX267 clinical trial.
- Patients who are allergic to compounds that are similar to NGX267.
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00637793
Locations
| United States, Pennsylvania | |
| Altoona Center for Clinical Research | |
| Duncansville, Pennsylvania, United States, 16635 | |
| Penn Rheumatology Associates and Sjogren's Syndrome Center | |
| Philadelphia, Pennsylvania, United States, 19104 | |
| United States, Texas | |
| Walter F. Chase MD PA | |
| Austin, Texas, United States, 78705 | |
Sponsors and Collaborators
TorreyPines Therapeutics
Investigators
| Principal Investigator: | Walter F. Chase, M.D. | Walter F. Chase MD. PA |
| Principal Investigator: | Alan Kivitz, M.D. | Altoona Center for Clinical Research |
| Principal Investigator: | Frederick B. Vivino, M.D. | Penn Rheumatology Associates and Sjogren's Syndrome Center |
More Information
No publications provided
| Responsible Party: | Susan Mellberg, R.N., M.B.A.; VP, Project Management, TorreyPines Therapeutics, Inc. |
| ClinicalTrials.gov Identifier: | NCT00637793 History of Changes |
| Other Study ID Numbers: | NGX267XSS2001 |
| Study First Received: | March 11, 2008 |
| Last Updated: | January 28, 2009 |
| Health Authority: | United States: Food and Drug Administration |
Keywords provided by TorreyPines Therapeutics:
|
Xerostomia Sjogren's Syndrome |
Additional relevant MeSH terms:
|
Xerostomia Sjogren's Syndrome Salivary Gland Diseases Mouth Diseases Stomatognathic Diseases Arthritis, Rheumatoid Arthritis Joint Diseases |
Musculoskeletal Diseases Rheumatic Diseases Dry Eye Syndromes Lacrimal Apparatus Diseases Eye Diseases Connective Tissue Diseases Autoimmune Diseases Immune System Diseases |
ClinicalTrials.gov processed this record on May 16, 2013