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AD 237

Phase 2

COPD | Small molecule | Respiratory |Novartis AG|Trials Updated: May 16, 2006

AD 237 development status

Highest phase Phase 2
Registered trials 1 across 1 sponsor since Oct 2005

Success Probability

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Market & Valuation

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Trial Design

RandomizedDouble-BlindUNCONTROLLED
Total Trials1
Total Enrollment300

FDA Designations

No designations recorded

AD 237 clinical trials

AD 237 · 1 trial · 1 indication

Phase 2 1
NCT00242333A Study to Assess the Safety and Efficacy of Different AD 237 Doses in Adults With COPDCOPD
COMPLETED300 Analytics
PHASE2COMPLETED
A Study to Assess the Safety and Efficacy of Different AD 237 Doses in Adults With COPD
COPDUnlock trial analytics

Study Endpoints

Primary Endpoints

Pulmonary function

Secondary Endpoints

Pulmonary function
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Study Design & Arms

AllocationRANDOMIZED
MaskingDOUBLE
ModelPARALLEL
PurposeTREATMENT

Interventions

NameTypeDescription
AD 237DRUG -
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Eligibility Criteria

Age Range40 Years to N/A
SexALL
Healthy VolunteersNo
Study Sites33

Inclusion Criteria: * Diagnosed with COPD, with symptoms of cough and chronic sputum production and/or dyspnea. * Post-bronchodilator FEV1 at no more than 65% and at least 30% of the predicted normal value. * Pre-bronchodilator FEV1/FVC ratio of less than 70%. * Current or ex-smokers with a smoking...

Countries:BulgariaHungaryPolandRomania
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