跳至主要内容
临床试验/NCT05844449
NCT05844449Enrolling By Invitation3 期

A Phase 3, Open-label Study Evaluating the Long-term Safety and Efficacy of Vanzacaftor/Tezacaftor/Deutivacaftor Triple Combination Therapy in Cystic Fibrosis Subjects 1 Year of Age and Older

Vertex Pharmaceuticals Incorporated54 个研究点 分布在 9 个国家目标入组 174 人开始时间: 2023年8月11日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
Enrolling By Invitation
入组人数
174
试验地点
54
主要终点
Part A: Safety and Tolerability as Assessed by Number of Participants With Adverse Events (AEs)

研究概览

简要总结

The purpose of this study is to evaluate the long-term safety, tolerability, and efficacy of vanzacaftor/tezacaftor/deutivacaftor (VNZ/TEZ/D-IVA) in participants with cystic fibrosis (CF).

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
1 Year 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Parts A and B:
  • Participants who have completed study drug treatment in the parent study (VX21-121-105; NCT Number: NCT05422222)
  • Meets at least 1 of the following criteria:
  • Completed study drug treatment in Part A
  • Had study drug interruption(s) in Part A, but did not permanently discontinue study drug and completed study visits up to the last scheduled visit of the treatment period of Part A

排除标准

  • Hepatic cirrhosis with portal hypertension, moderate hepatic impairment, or severe hepatic impairment that might pose an additional risk in administering study drug
  • History of solid organ, hematological transplantation, or cancer
  • History of drug intolerance in the parent study
  • Other protocol defined Inclusion/Exclusion criteria may apply.

研究组 & 干预措施

VNZ/TEZ/D-IVA

Experimental

Part A: Participants (Cohort 1: 6 through 11 years of age (inclusive); Cohort 2: 2 through 5 years of age (inclusive) and Cohort 3: 1 to less than (<) 2 years of age) will receive VNZ/TEZ/D-IVA once daily at doses determined based on their age and weight. The age range is based on date of informed consent in parent study.

Part B: Participants in Cohort 1 who meet the eligibility criteria will receive VNZ/TEZ/D-IVA for an additional 96 weeks.

干预措施: VNZ/TEZ/D-IVA (Drug)

结局指标

主要结局

Part A: Safety and Tolerability as Assessed by Number of Participants With Adverse Events (AEs)

时间窗: From Baseline up to Week 100

Part B: Safety and Tolerability as Assessed by Number of Participants With Adverse Events (AEs)

时间窗: From Baseline up to Week 196

次要结局

  • Part A (All Cohorts): Absolute Change in Sweat Chloride (SwCl)(From Baseline Through Week 96)
  • Part B: Absolute Change in Sweat Chloride (SwCl)(From Baseline Through Week 192)
  • Part A (Cohort 1): Absolute Change in Percent Predicted Forced Expiratory Volume (ppFEV1)(From Baseline Through Week 100)
  • Part B: Absolute Change in Percent Predicted Forced Expiratory Volume (ppFEV1)(From Baseline Through Week 196)
  • Part A (All Cohorts): Number of Pulmonary Exacerbation (PEx)(From Baseline Through Week 100)
  • Part B: Absolute Change in Body Mass Index (BMI)(From Baseline Through Week 196)
  • Part A (Cohorts 1 and 2): Absolute Change in BMI-for-age Z-score(From Baseline Through Week 100)
  • Part B: Number of Pulmonary Exacerbation (PEx)(From Baseline Through Week 196)
  • Part A (All Cohorts): Number of CF- Related Hospitalizations(From Baseline Through Week 100)
  • Part B: Number of CF- Related Hospitalizations(From Baseline Through Week 196)
  • Part A (Cohort 1): Absolute Change in Cystic Fibrosis Questionnaire-Revised (CFQ-R) Respiratory Domain (RD) Score(From Baseline Through Week 100)
  • Part B: Absolute Change in Cystic Fibrosis Questionnaire-Revised (CFQ-R) Respiratory Domain (RD) Score(From Baseline Through Week 196)
  • Part A (Cohorts 1 and 2): Absolute Change in Body Mass Index (BMI)(From Baseline Through Week 100)
  • Part B: Absolute Change in BMI-for-age Z-score(From Baseline Through Week 196)
  • Part A (Cohort 3): Absolute Change in Weight-for-length(From Baseline Through Week 100)
  • Part B: Absolute Change in Weight-for-length(From Baseline Through Week 196)
  • Part A (Cohort 3): Absolute Change in Weight-for-length Z-score(From Baseline Through Week 100)
  • Part B: Absolute Change in Weight-for-length Z-score(From Baseline Through Week 196)
  • Part A (All Cohorts): Absolute Change in Weight(From Baseline Through Week 100)
  • Part B: Absolute Change in Weight(From Baseline Through Week 196)
  • Part A (All Cohorts): Change in Weight-for-age Z-score(From Baseline Through Week 100)
  • Part B: Change in Weight-for-age Z-score(From Baseline Through Week 196)
  • Part A (Cohorts 1 and 2): Absolute Change in Height(From Baseline Through Week 100)
  • Part B: Absolute Change in Height(From Baseline Through Week 196)
  • Part A (Cohorts 1 and 2): Absolute Change in Height-for-age Z-score(From Baseline Through Week 100)
  • Part B: Absolute Change in Height-for-age Z-score(From Baseline Through Week 196)
  • Part A (Cohort 3): Absolute Change in Length(From Baseline Through Week 100)
  • Part B: Absolute Change in Length(From Baseline Through Week 196)
  • Part A (Cohort 3): Absolute Change in Length-for-age Z-score(From Baseline Through Week 100)
  • Part B: Absolute Change in Length-for-age Z-score(From Baseline Through Week 196)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (54)

Loading locations...

相似试验