Clinical Trials Logo

Clinical Trial Summary

The purpose of this study is to investigate the potential effects of cladribine on the pharmacokinetics of monophasic oral contraceptive microgynon® by assessment of its constituents, ethinyl estradiol (EE) and levonorgestrel (LNG).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04086225
Study type Interventional
Source Merck Healthcare KGaA, Darmstadt Germany, an affiliate of Merck KGaA, Darmstadt, Germany
Contact Communication Center
Phone +49 6151 72 5200
Email service@emdgroup.com
Status Recruiting
Phase Phase 1
Start date January 17, 2019
Completion date April 6, 2020

See also
  Status Clinical Trial Phase
Completed NCT03277261 - Study to Assess the Efficacy and Safety of Ublituximab in Participants With Relapsing Forms of Multiple Sclerosis (RMS) ( ULTIMATE 1 ) Phase 3
Active, not recruiting NCT04130997 - An Extension Study of Ublituximab in Participants With Relapsing Multiple Sclerosis Phase 3
Completed NCT02921035 - Non-interventional Study to Assess Adherence to Treatment for Patients With RMS (MAIN-MS)
Completed NCT04878211 - A Open-label Study to Assess Response to COVID-19 Vaccine in Multiple Sclerosis Participants Treated With Ofatumumab Phase 4
Completed NCT03745144 - Effects of Cladribine Tablets on the PK of Microgynon® Phase 1
Active, not recruiting NCT04667949 - Study of Efficacy and Safety of Fingolimod (Gilenya) 0.5 mg in Chinese Patients With Relapsing Multiple Sclerosis (RMS) Patients Phase 4
Completed NCT03277248 - Study to Assess the Efficacy and Safety of Ublituximab in Participants With Relapsing Forms of Multiple Sclerosis (RMS) Phase 3