Short Term Effects of Ivacaftor in Non-G551D Cystic Fibrosis Patients

Ivacaftor is a cystic fibrosis (CF)channel potentiator that is associated with decreased sweat chloride concentration, improved lung function, and improved weight gain. It is currently FDA approved for use only in CF patients with the G551D gating mutation. In vivo data suggest that ivacaftor may potentiate CF channels coded for by many other mutations associated with residual channel function, i.e., that some CF protein is present in the cell membrane of affected cells. This includes all of the 9 other known gating mutations, but ivacaftor also may be effective in CF patients with non-gating mutations, including some associated with severe phenotype. Based on results from previous studies, we hypothesize that non-G551D patients with signs of residual CF channel activity might respond favorably to treatment with ivacaftor. This includes patients with any of the non-G551D gating mutations, that are pancreatic sufficient, that have a sweat chloride concentration between 55 and 85 mmol, or that are much healthier than expected. Hence, select CF patients treated with ivacaftor as compared to placebo will have a decrease in sweat chloride concentration by greater than 20 mmol, improvement in FEV1, and weight gain. To test our hypothesis, we will conduct a prospective double-blinded placebo-controlled crossover clinical study comparing treatment with ivacaftor to placebo therapy (see details below). Our specific aims are: Specific Aim 1: To demonstrate a decrease in sweat chloride concentration by greater than 20 mmol from baseline after 14 days of ivacaftor as compared to placebo. Specific Aim 2: To demonstrate improvement in lung function measures from baseline after 14 days of Ivacaftor as compared to placebo. Specific Aim 3:To demonstrate weight gain from baseline after 14 days of Ivacaftor as compared to placebo. Study Design: This is a prospective randomized double-blinded placebo-controlled crossover study of the short-term effects of ivacaftor (aka VX-770 or Kalydeco) on sweat chloride concentration and lung function in cystic fibrosis (CF) patients who fall outside current FDA approval. We will enroll up to 30 CF subjects from the UCSF CF Center with a variety of genotypes and phenotypes in which there is one or more signs of residual CFTR function. The signs of residual CF channel function include: pancreatic sufficiency, sweat chloride concentration less than 85 mmol, or milder than expected CF disease in a CF patient with a severe genotype. We will exclude patients who are homozygous for the F508del mutation and have a sweat chloride concentration greater 85 mmol, which is true of the majority of F508del homozygotes. This population has been studied and found to be unresponsive to ivacaftor and includes nearly half of all CF patients. However, even among F508del homozygotes about 15 percent have residual chloride secretion manifest as a lower than expected sweat chloride concentration. The primary outcome measure will be the difference in sweat chloride concentration measured in subjects on placebo and on ivacaftor. Secondary outcome measures include variables obtained by spirometry and multi-breath washout testing. Research Plan: We will conduct a randomized double-blinded placebo-controlled crossover trial, in which all subjects will be treated with 2 weeks of ivacaftor and 2 weeks of placebo with a 2-week wash out period. Up to 30 subjects with one or more signs of residual CFTR function will be randomized into the study. This includes subjects who are pancreatic sufficient, who have a sweat chloride of 55 to 85 mmol, or who have mild CF disease in a setting of a severe CF genotype. Each subject will act as his/her own control in a prospective randomized double-blinded crossover trial consisting of 14 days of ivacaftor or placebo, followed by a 14 day washout period, followed by 14 days of placebo or ivacaftor. The primary outcome measure will be sweat chloride concentration at baseline, 14 days, 28 days and 42 days. Secondary outcomes include standard lung function measures: forced vital capacity (FVC), forced expiratory volume at 1 second (FEV1), FEV1/FVC and mid-expiratory flow (FEF25-75), and multibreath washout testing. Blood samples will be examined at baseline, 14 days, 28 days and 42 days for evidence of drug toxicity (CBC with differential, liver function tests (AST, ALT), non-fasting glucose, creatinine and BUN). For female subjects of child bearing age, a urine pregnancy test will be done to assure they are not pregnant. If a female becomes pregnant during the study, the trial will be stopped but we will continue to measure sweat chloride, lung function, and blood work at the specified times. The effects of ivacaftor on the fetus are not known at this time. Results of all laboratory tests will be forwarded to a nurse practitioner not directly involved with the study subjects, who will serve as the subject safety monitor. The nurse practitioner will notify study investigators of any laboratory values consistent with an adverse effect of study drug and will have the power to discontinue any subject in case of a serious adverse event. The most common serious adverse event in previous ivacaftor trials was mild elevation of liver tests. For this trial a serious adverse event sufficient to warrant discontinuing a subject will include a liver function test (ALT or AST) more than thrice the upper limit of normal, abnormal renal function or abnormal red or white cell counts.