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A Trial Study of SGN-00101 in Treating Pediatric Patients With Recurrent Respiratory Papillomatosis

Phase 2
Completed
Conditions
Papilloma
Recurrent Respiratory Papillomatosis
Registration Number
NCT00038714
Lead Sponsor
Nventa Biopharmaceuticals Corporation
Brief Summary

Recurrent Respiratory Papillomatosis (RRP) causes wart-like lesions along the throat area and can obstruct the airway or become malignant. The cause has been related to specific types of Human Papillomavirus (HPV). The purpose of the study is to assess the clinical effectiveness of a trial drug, SGN-00101, in children with RRP and also assess its safety.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
27
Inclusion Criteria
  • Male or female between 2 and 18 yrs old, inclusive, who has documented RRP.
  • Patients with documented RRP
  • Subject is surgically debulked within 7 days before the first dose of SGN-00101.
  • Subject has had at least 4 debulking surgeries for RRP, had no intersurgical intervals greater than 84 days during the period of the last 4 surgeries.
  • Subject is free of life threatening or serious concomitant disorders other than the disease under study.
  • Females of childbearing potential must have a negative pregnancy test and must be practicing an effective/appropriate method of birth control as determined by the Investigator.
Exclusion Criteria
  • Subject has disease or status that causes compromise of the immune system.
  • Subject has a history of ionizing radiation therapy to the respiratory tract.
  • Patient has used concomitant medications that may suppress the immune system.
  • Subject has received any specific or non-specific immunotherapy intended as treatment for their RRP (i.e. mumps vaccine injected intralesionally) within 9 months prior to Week 0 of this study.
  • Subject has participated in a past study with SGN-00101
  • Pregnancy and lactation.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (8)

Fairview University Medical Center, University of Minnesota

🇺🇸

Minneapolis, Minnesota, United States

University Hospitals of Cleveland

🇺🇸

Cleveland, Ohio, United States

Nemour's Childrens Clinic, Division of Pediatric Oncology

🇺🇸

Jacksonville, Florida, United States

Children's Hospital of the King's Daughters

🇺🇸

Norfolk, Virginia, United States

Children's Hospital of Alabama

🇺🇸

Birmingham, Alabama, United States

University of Arkansas for Medical Sciences, Arkansas Children's Hospital

🇺🇸

Little Rock, Arkansas, United States

University of Iowa Hospitals and Clinics

🇺🇸

Iowa City, Iowa, United States

University of Texas, Southwestern Medical School

🇺🇸

Dallas, Texas, United States

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