Recent Updates
Recently added Catalysts

BSF 208075

Phase 2

Pulmonary Hypertension | Small molecule | Cardiovascular |Gilead Sciences, Inc.|Last Updated: Apr 16, 2009

Success Probability
Approval Probability 71%
TA Base Rate26%
Adjusted LOA41%
ML RiskLOW_RISK
Premium
Market & Valuation
rNPV $3.2B
Market Size $9.4B
Revenue Basis $1.6B
Competitors 6
Premium
Trial Design
RandomizedDouble-BlindUNCONTROLLEDBiomarker
Total Trials1
Total Enrollment60
FDA Designations
No designations recorded
Clinical Trials (1)
NCT IDTitlePhaseStatusEnrollmentVelocityDesignStartCompletionLast UpdatedSitesCountries
NCT00046319Study of BSF 208075 Evaluating Exercise Capacity in Patients With Pulmonary Arterial HypertensionPHASE2 COMPLETED 60Sep 1, 2002Jun 1, 2003Apr 16, 200921 United States, Australia +4
Unlock Drug Trial Details
Study Endpoints
Primary Endpoints
Change from baseline to Week 12 in six minute walk distance
Secondary Endpoints
Change from baseline to Week 12 in:
Borg Dyspnea Index
WHO Functional Classification
Unlock Study Endpoints
Study Design & Arms
AllocationRANDOMIZED
MaskingDOUBLE
ModelPARALLEL
PurposeTREATMENT
Interventions
NameTypeDescription
BSF 208075DRUG -
Unlock Study Design Details
Eligibility Criteria
Age Range18 Years — N/A
SexALL
Healthy VolunteersNo
Study Sites21

--Disease Characteristics-- * Current diagnosis of either PPH or PAH secondary to the scleroderma spectrum of disease (e.g., mixed connective tissue disease, systemic lupus erythematosus, systemic sclerosis, or overlap syndrome), anorexigen use, or human immunodeficiency virus (HIV) infection at th...

Countries:United StatesAustraliaBelgiumFranceGermanyItaly
Unlock Eligibility Criteria