跳至主要内容
临床试验/NCT00143247
NCT00143247终止2 期

An Open-Label, Phase 2, Long-Term Safety Study of Inhaled Insulin: An Up to Four-Year Extension of Therapy in Subjects With Type 1 or Type 2 Diabetes Mellitus Participating in Extension Protocols 217-102, 103, or 104

Pfizer1 个研究点 分布在 1 个国家目标入组 173 人开始时间: 2003年3月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
终止
发起方
Pfizer
入组人数
173
试验地点
1
主要终点
Change in Forced Expiratory Volume in 1 Second (L) by Time on Exubera Treatment

研究概览

简要总结

This is a long-term safety study for Phase 2 subjects who choose to remain on Exubera® (inhaled insulin).

详细描述

The study was terminated on Oct. 18, 2007. This study is not a post approval commitment study. Pfizer decided to cancel new trials because of the decision to withdraw Exubera® (inhaled insulin) due to lack of market performance and not for safety reasons.

研究设计

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

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Subjects with Type 1 or Type 2 Diabetes Mellitus who participated in previous Phase 2 extension protocols

排除标准

  • Pregnancy

研究组 & 干预措施

Exubera® (inhaled insulin)

Experimental

Open label, no comparator

干预措施: Exubera® (inhaled insulin) (Drug)

结局指标

主要结局

Change in Forced Expiratory Volume in 1 Second (L) by Time on Exubera Treatment

时间窗: Baseline to 126 months

Change from Baseline: mean of (value of observed forced expiratory volume in 1 second (FEV1) (liters) at treatment duration minus baseline value). Duration of treatment is based on the elapsed duration of treatment in the controlled and uncontrolled studies. Baseline was based on pre-inhaled insulin measurements.

Change in Carbon Monoxide Diffusing Capacity (mL/Min/mm Hg) by Time on Exubera Treatment

时间窗: baseline to 126 months

Change from Baseline: mean of (value of observed Carbon Monoxide Diffusing Capacity (mL/min/mm Hg) at treatment duration minus baseline value). Duration of treatment is based on the elapsed duration of treatment in the controlled and uncontrolled studies. Baseline was based on pre-inhaled insulin measurements.

次要结局

  • Hypoglycemic Event Rates by Interval of Exubera Treatment(0 to 132 months)
  • Severe Hypoglycemic Event Rates by Interval of Exubera Treatment(0-132 months)
  • Insulin Antibodies (Percent Binding) by Time on Exubera Treatment - Subjects With Type 1 Diabetes(36 months to 126 months)
  • Insulin Antibodies (Percent Binding) by Time on Exubera Treatment - Subjects With Type 2 Diabetes (Using Insulin at Study Entry)(36 to 126 months)
  • Insulin Antibodies (Percent Binding) by Time on Exubera Treatment - Subjects With Type 2 Diabetes (Not Using Insulin at Study Entry)(6 to 120 months)
  • Number of Decliners in Either Forced Expiratory Volume in 1 Second (L) or Carbon Monoxide Diffusing Capacity (ml/Min/mm Hg), by Duration of Exubera Treatment(3 to >=108 months)
  • Number of Decliners in Forced Expiratory Volume in 1 Second (L) by Duration of Exubera Treatment(3 to >=108 months)
  • Number of Decliners in Carbon Monoxide Diffusing Capacity (ml/Min/mm Hg) by Duration of Exubera Treatment(6 to >=108 months)
  • Change in Glycosylated Hemoglobin by Duration of Exubera Treatment(Baseline to 126 months)

研究者

发起方
Pfizer
申办方类型
Industry

研究点 (1)

Loading locations...

相似试验

终止
2 期
[S,S]-Reboxetine Long Term Safety Study In Post-Shingles Pain.Pain
NCT00354094Pfizer600
已完成
2 期
Open Label Extension Study of Epratuzumab in Japanese Systemic Lupus Erythematosus (SLE) SubjectsSystemic Lupus Erythematosus
NCT01534403UCB Pharma17
已完成
2 期
Open-Label Extension Study of Patients Previously Enrolled in Study CIN-107-124Hypertension
NCT05459688AstraZeneca175
进行中(未招募)
2 期
Phase 2 Open-label Extension Study of AOC 1020 in Participants With Facioscapulohumeral Muscular Dystrophy (FSHD)FSHDFSHD1FSHD2FMDFMD2Fascioscapulohumeral Muscular DystrophyFascioscapulohumeral Muscular Dystrophy Type 1Fascioscapulohumeral Muscular Dystrophy Type 2Dystrophies, Facioscapulohumeral MuscularDystrophy, Facioscapulohumeral MuscularFacioscapulohumeral Muscular Dystrophy 1Facioscapulohumeral Muscular Dystrophy 2Facio-Scapulo-Humeral DystrophyAtrophy, FacioscapulohumeralAtrophies, FacioscapulohumeralFacioscapulohumeral AtrophyMuscular DystrophiesMuscular Dystrophy, FacioscapulohumeralFSH Muscular DystrophyLandouzy Dejerine DystrophyLandouzy-Dejerine Muscular DystrophyDystrophies, Landouzy-DejerineDystrophy, Landouzy-DejerineLandouzy-Dejerine SyndromeMuscular Dystrophy, Landouzy DejerineFSHProgressive Muscular Dystrophy
NCT06547216Avidity Biosciences, Inc.84
进行中(未招募)
2 期
Phase 2, Open-label, Long-term study of the safety and efficacy of TM5614 in combination with tyrosine kinase inhibitors in chronic phase chronic myelogenous leukemia patientsChronic myelogenous leukemia in chronic phaseCMLD015464
JPRN-jRCT2031190071Harigae Hideo35