Study of Celebrex (Celecoxib) in Patients With Recurrent Respiratory Papillomatosis

Northwell Health

Status and phase: Completed; Phase 2

Conditions: Recurrent Respiratory Papillomatosis

Treatments: Drug: celebrex (celecoxib); Drug: placebo

Study type: Interventional

Funder types: Other; NIH

Identifiers

NCT00571701

1U01DC007946-01A2 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

This is a randomized double blind controlled study to determine if celebrex (celecoxib), a selective COX-2 inhibitor, can decrease the rate of recurrence in adult and pediatric patients with recurrent respiratory papillomatosis. All patients will be evaluated for disease severity at enrollment and at 3 month intervals for 30 months. After randomization, patients in the early treatment arm will begin celecoxib 6 months after enrollment. The delayed treatment arm will begin celecoxib 18 months after enrollment. All patients will receive celecoxib for 1 year. During the time that patients do not receive celecoxib, they will receive a placebo capsule with the same appearance. Follow-up visits will occur at three month intervals for the duration of the study.

Full description

This is a randomized double blind placebo-controlled study,with plans to include 5 additional U.S. centers in the near future. The primary goal of this study is to determine whether celecoxib has efficacy in elimination or reduction of recurrent disease in patients with RRP. Our secondary goals are to determine whether continued celecoxib is required to maintain response, to correlate response with select patient demographics and with plasma levels of celecoxib. The study design encompasses a 30-month period, which can be divided into three segments:

Segment A: This is a 6 month run-in period in which all patients are assessed by direct laryngoscopy/bronchoscopy for disease severity, to permit growth rate stabilization and confirm accuracy of training of participating physicians. Patients will be treated by conventional surgery at three months and six months after enrollment.

Segment B: Patients begin 12 months of 400mg(adults), 100 mg (pediatric weight between 12 and 25 kg)or 200 mg (pediatric weight > 25kg) celecoxib daily or placebo treatment in addition to surgical removal of all papillomas at each 3 month interval. This segment directly tests the hypothesis that celecoxib is an efficacious treatment for moderate to severe RRP and forms the basis for the primary statistical analyses.

Segment C: The primary purpose of this segment is to determine whether gains made during celecoxib therapy are maintained after it is discontinued, or whether celecoxib will need to be taken indefinitely. This will be determined by a 12 month period on placebo after cessation of celecoxib for the early treatment group. This is not a traditional cross-over study because we expected a sustained effect therefore no efficacy studies were done in segment C. However, the placebo first group was given celecoxib so that they could gain any possible benefits equivalent to those that received the celecoxib first.

Enrollment: 50 patients

Sex: All

Ages: 2+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Moderate to severe disease, defined as:

Patients who have rapid regrowth of papillomas, requiring endoscopic removal at least 3 times within the past 12 months AND A papilloma growth rate from 0.03 to 0.06 (moderate) or >0.06 (severe) at time of initial direct endoscopy OR Having tracheal and/or bronchial or pulmonary papillomatosis (severe)

• Age > 2 years
• Gender- no restriction
• Race- no restriction

Exclusion criteria

• Fewer than 3 surgical procedures in previous year, without tracheal disease
• Age < 2 years
• Pregnancy, trying to become pregnant, breastfeeding or not willing to comply with birth control methods if sexually active female
• Serum creatinine > 1.5 X normal
• History of documented peptic ulcer disease or gastritis persisting despite treatment
• Abnormal liver function tests, as total bilirubin >1.5 X normal and SGOT > 3 X normal
• Allergy to NSAIDs, sulfa containing drugs or symptoms of Stevens-Johnson Syndrome
• Patients with connective tissue diseases such as SLE, Raynaud's or Systemic Sclerosis
• Patients with known diabetes
• Patients on warfarin, or on loop or thiazide diuretics
• Patients with a history of cardiovascular disease, myocardial infarct or stroke
• Patients with congestive heart failure
• Patients regularly taking > 81 mg of aspirin/day
• Patients with uncontrolled hypertension
• Patients with RRP associated malignancy currently receiving chemotherapy and/or radiation

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Crossover Assignment

Masking: Quadruple Blind

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50 participants in 2 patient groups, including a placebo group

celecoxib first, then placebo

Active Comparator group

Description:

Patients randomized to start celecoxib 6 months after enrollment. Then cross over to placebo after 1 year. Celecoxib dosing will be given orally 400mg once a day for adults, 200 mg once a day for pediatric patients between 12-25kg, 100mg once a day for pediatric patients \< 12kg

Treatment:

Drug: placebo

Drug: celebrex (celecoxib)

Placebo first, then celecoxib

Placebo Comparator group

Description:

Patients randomized to start placebo 6 months after enrollment. One placebo capsule will be taken orally once a day. Placebo will match appearance of active celecoxib capsules. Cross over to 12 months of treatment with celecoxib after 1 year.

Treatment:

Drug: placebo

Drug: celebrex (celecoxib)