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NCT01405157

A Bioequivalence Study Comparing Methylprednisolone Suspension To Methylprednisolone Tablets Under Fasting Conditions

Withdrawn Phase 1 Last updated 23 October 2018
What this trial tests

Phase 1 trial testing methylprednisolone in Therapeutic Equivalency. Withdrawn.

Timeline
1 January 2012
Primary endpoint
20 February 2012
20 February 2012

Quick facts

Lead sponsorPfizer
PhasePhase 1
StatusWithdrawn
Study typeINTERVENTIONAL
Allocationrandomized
Designcrossover
Maskingnone
Primary purposebasic science
Start date1 January 2012
Primary completion20 February 2012
Estimated completion20 February 2012

Drugs / interventions tested

Conditions studied

Sponsor

Pfizer — full company profile →

Who can join

Adults 21 to 55, any sex, with Therapeutic Equivalency. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

A study to determine whether a new formulation of methylprednisolone suspension is bioequivalent to methylprednisolone tablets under fasting conditions.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of methylprednisolone

Trials testing the same drug.

Other Pfizer trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT01405157.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing