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Merimepodib

Phase 2

Hepatitis C | Small molecule | Infectious Disease |Vertex Pharmaceuticals Incorporated|Trials Updated: Dec 21, 2007

Merimepodib development status

Highest phase Phase 2
Registered trials 2 across 2 sponsors since Jul 2004

Merimepodib target and mechanism

Molecular targetIMPDH1
Target classInhibitor
ModalitySmall molecule

Success Probability

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Market & Valuation

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Trial Design

RandomizedDouble-BlindUNCONTROLLED
Total Trials1
Total Enrollment315

FDA Designations

No designations recorded

Merimepodib clinical trials

Merimepodib · 1 trial · 2 indications

Phase 2 1
NCT00088504Merimepodib (MMPD) in Triple Combination for the Treatment of Chronic Hepatitis CHepatitis C
COMPLETED315 Analytics
PHASE2COMPLETED
Merimepodib (MMPD) in Triple Combination for the Treatment of Chronic Hepatitis C
Hepatitis CUnlock trial analytics

Study Design & Arms

AllocationRANDOMIZED
MaskingDOUBLE
ModelPARALLEL
PurposeTREATMENT

Interventions

NameTypeDescription
MerimepodibDRUG -
PEG-Interferon-alpha 2a (Pegasys®)DRUG -
Ribavirin (Copegus®)DRUG -
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Eligibility Criteria

Age Range18 Years to 70 Years
SexALL
Healthy VolunteersNo
Study Sites67

Inclusion Criteria: The following is a summary of the inclusion and exclusion criteria for the Merimepodib Triple Combination (METRO) trial. There are also additional criteria, which will be reviewed with you by the staff at the clinical study site, to make sure you are eligible for the study. Some...

Countries:United States
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Competitive Landscape -Hepatitis C 13 trials

Top 1 of 4 competitors

CompanyTickerTrialsLead PhaseDrugs
Atea Pharmaceuticals, Inc.AVIR2PHASE3Bemnifosbuvir-Ruzasvir
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Frequently asked questions about Merimepodib

What is Merimepodib used for?

Merimepodib is an investigational small molecule developed for the treatment of chronic hepatitis C, a viral infection of the liver. It was studied as part of a triple combination regimen in adults 18 years and older. It is not an approved therapy and remains in clinical development.

What does Merimepodib target?

Merimepodib targets IMPDH1, inosine monophosphate dehydrogenase 1, and acts as an inhibitor of that enzyme. Inhibiting IMPDH1 interferes with guanine nucleotide synthesis, which is a pathway the hepatitis C virus relies on for replication. This mechanism is distinct from direct-acting antiviral approaches.

Who is developing Merimepodib?

Merimepodib was developed by Vertex Pharmaceuticals Incorporated, which trades on the Nasdaq under the ticker VRTX. Vertex sponsored the clinical program evaluating the compound in chronic hepatitis C. The drug is an investigational small molecule and is not a marketed product.

What phase is Merimepodib in?

Merimepodib reached Phase 2 clinical development for chronic hepatitis C. It is an investigational agent and is not FDA approved. The Phase 2 program has concluded, with one completed trial and no active trials currently listed for the compound.

What clinical trials is Merimepodib in?

Merimepodib was evaluated in the Phase 2 trial NCT00088504, titled Merimepodib (MMPD) in Triple Combination for the Treatment of Chronic Hepatitis C. The trial enrolled 315 participants across sites in the United States, used a randomized, double-blind design, and has been completed.

Is Merimepodib biomarker selected?

No. Merimepodib was studied in chronic hepatitis C without biomarker-based patient selection. The Phase 2 trial NCT00088504 enrolled adults 18 years and older of all sexes, excluded healthy volunteers, and did not restrict enrollment to a biomarker-defined subgroup of patients.