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BmDR

Biomarker Data Repository

MSOAC

Multiple Sclerosis Outcome Assessments Consortium

CPAD

Critical Path For Alzheimer’s Disease

PRO Consortium

Patient-Reported Outcome Consortium

CPP

Critical Path for Parkinson’s

PKDOC

Polycystic Kidney Disease Outcomes Consortium

CP-RND

Critical Path for Rare Neurodegenerative Diseases

PredicTox KE

PredicTox Knowledge Environment

CP-SCD

Critical Path for Sickle Cell Disease

PSTC

Predictive Safety Testing Consortium

CPTA

Critical Path to Therapeutics for the Ataxias

QuantMed

Quantitative Medicine Program

CDRC

CURE Drug Repurposing Collaboratory

RDCA-DAP

Rare Disease Cures Accelerator-Data and Analytics Platform

DCC

Data Collaboration Center

RD-COA Consortium

Rare Disease Clinical Outcome Assessment Consortium

D-RSC

Duchenne Regulatory Science Consortium

TB-PACTS

TB-Platform for Aggregation of Clinical TB Studies

eCOA Consortium

Electronic Clinical Outcome Assessment Consortium

TTC

Transplant Therapeutics Consortium

FA-ICD

Friedreich’s Ataxia Integrated Clinical Database

TOMI-T1D

Trial Outcome Markers Initiative in T1D Consortium

HD-RSC

Huntington’s Disease Regulatory Science Consortium

TRxA

Translational Therapeutics Accelerator

INC

International Neonatal Consortium

T1D

Type 1 Diabetes Consortium

Completed Consortia

CFAST

Coalition for Accelerating Standards & Therapies

PTC

Pediatric Trials Consortium

CPTR

Critical Path to TB Drug Regimens
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Home>News & Events>October 10, 2016

News

September 18, 2017 PRINT PDF

October 10, 2016

CPP obtains EMA regulatory support for use of imaging biomarker in PD clinical trials

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