Study of TD101, a Small Interfering RNA (siRNA) Designed for Treatment of Pachyonychia Congenita

Pachyonychia Congenita Clinical Trial

Official title:

A Single-Center, Placebo-Controlled, Rising Dose to Tolerance and Safety Study of TD101, an siRNA Designed for Treatment of Pachyonychia Congenita

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00716014
• Other study ID #: 24013
• Status: Completed
• Phase: Phase 1
• First received: July 15, 2008
• Last updated: November 18, 2008
• Start date: January 2008
• Est. completion date: August 2008

Study information

• Verified date: November 2008
• Source: Pachyonychia Congenita Project
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

Pachyonychia congenita (PC) is a rare, autosomal dominant keratin disorder affecting the nails, skin, oral mucosae, larynx, hair and teeth. Pathogenic mutations in keratin K6a, K6b, K16 or K17 act via a dominant negative mechanism, leading to manifestations of the disease. The most disabling PC symptom is a painful plantar blistering and keratoderma that requires use of ambulation devices in more than 50 percent of patients. Despite our understanding of the molecular basis of PC, current treatment is limited to mechanical removal of the thick calluses, non-specific topical keratolytics, and oral retinoids, none of which alleviates blistering or plantar pain satisfactorily. A public charity, PC Project, has been founded to support the development of treatments for PC (www.pachyonychia.org). In collaboration with this charity, a small company, TransDerm, Inc., has developed a small interfering RNA (siRNA) that specifically targets a mutation in one of the PC keratins, K6a. As this siRNA targets a single nucleotide mutation, it will only be effective against PC subjects harboring this specific mutation. There are currently only six known patients who carry this mutation in the International Pachyonychia Congenita Research Registry, but three of these patients live in Salt Lake City (a mother and two of her children). We propose to perform a Phase Ib clinical trial to test the safety and tolerability of TD101 in PC patients carrying an N171K mutation. We will complete treatment of the adult patient prior to recruitment of the minors.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 1
• Est. completion date: August 2008
• Est. primary completion date: August 2008
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 10 Years and older

Eligibility

Inclusion Criteria:

• A positive genetic identification of the N171K mutation in the keratin 6a gene from a CLIA certified laboratory;

• Witnessed, signed informed consent approved by Institutional Review Board/Ethics Committee;

• A signed Health Information Portability and Accountability Act (HIPAA) authorization form which permits the use and disclosure of patient's individually identifiable health information for those enrolled in the United States of America;

• Male or female subjects of any race 10 years of age and older;

• Complete physical examination and medical history indicating no abnormalities that will interfere with study objectives;

• Normal or not clinically significant baseline laboratory tests, including hemogram, ANA, serum chemistry panel, urinalysis, C3a, Bb, and APTT,PT;

• Negative pregnancy test (females only).

Exclusion Criteria:

• Females of childbearing potential not using a highly effective method of birth control (e.g. implants, injectables, combined oral contraceptives, some intrauterine contraceptive devices) during the study;

• Diabetes mellitus requiring treatment other than diet and exercise;

• Treatment of any type for cancer within the last six months;

• History of any significant internal disease;

• Subjects who are known to be allergic to any of the test product(s) or any components in the test product(s) or history of hypersensitivity or allergic reactions to any of the study preparations;

• History of street drug or alcohol abuse;

• Any patient not able to meet the study attendance requirements;

• Subjects who have participated in any other trial of an investigational drug or device within 60 days prior to enrollment or participation in a research study concurrent with this study.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Pachyonychia Congenita

Intervention

Drug:
• TD101
TD101 is injection into a callus on the bottom of one of the patient's feet
• Normal saline (placebo)
A normal saline solution (placebo) is injected into one of the patient's feet.

Locations

Country	Name	City	State
United States	Huntsman Cancer Institute	Salt Lake City	Utah

Sponsors (1)

Lead Sponsor	Collaborator
Pachyonychia Congenita Project

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Determine safety/toxicity of TD101		18 weeks, followed by 3-month wash out period	Yes
Secondary	Determine efficacy of TD101		18 weeks, followed by 3-month wash out period	No