Relative Bioavailability (rBA) of Evobrutinib Intended Commercial and Clinical Tablets, and Effect of Food on Intended Commercial Tablets

Healthy Clinical Trial

Official title:

Phase I, Randomized, Open-Label, Single-Dose, Three Period, Six-Sequence Crossover Study to Determine the Relative Bioavailability of the Evobrutinib Intended Commercial Tablet Formulation (TF2) Compared to the Clinical Tablet Formulation (TF1) and Evaluate the Effect of Food on TF2 Bioavailability in Healthy Participants

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04314024
• Other study ID #: MS200527_0077
• Secondary ID: 2019-004738-40
• Status: Completed
• Phase: Phase 1
• Start date: May 25, 2020
• Est. completion date: June 23, 2020

Study information

• Verified date: July 2020
• Source: Merck Healthcare KGaA, Darmstadt, Germany, an affiliate of Merck KGaA, Darmstadt, Germany
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The study will evaluate the relative bioavailability (rBA) of the intended commercial tablet formulation (Test Treatment, TF2) of Evobrutinib compared to the clinical tablet formulation (Reference Treatment, TF1) of Evobrutinib and to assess the effect of food on the bioavailability of the intended commercial tablet formulation of Evobrutinib.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 18
• Est. completion date: June 23, 2020
• Est. primary completion date: June 23, 2020
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 55 Years

Eligibility

Inclusion Criteria:

• Participants are overtly healthy as medical evaluation, including no clinically significant abnormality identified on physical examination or laboratory evaluation and no active clinically significant disorder, condition, infection or disease that would pose a risk to participant safety or interfere with the study evaluation, procedures, or completion

• Male or female participants agree to be consistent with local regulations on contraception methods

• Female participants are not pregnant or breastfeeding, and at least one of the following condition applies:

• Not a WOCBP or

• If a WOCBP, use a highly effective contraceptive method (that is, with a failure rate of <1 percent per year, preferably with low user dependency for the following time period:

• Before the first dose of the study intervention, if using hormonal contraception:

• Has completed at least one 4-week cycle of an oral contraception pill and either had or has begun her menses or

• Has used a depot contraceptive or extended-cycle oral contraceptive for least 28 days and has a documented negative pregnancy test using a highly sensitive assay and

• A barrier method

• During the intervention period

• After the study intervention period (that is after the last dose of study intervention is administered) for at least 90 days, plus 30 days (a menstrual cycle) after the last dose of study intervention and agree not to donate eggs (ova, oocytes) for reproduction during this period. The Investigator evaluates the effectiveness of the contraceptive method in relationship to the first dose of study intervention

• Females have a negative serum pregnancy test at the Screening Visit and within 24 hours before the first dose of study intervention

• The Investigator reviews the medical history, menstrual history, and recent sexual activity to decrease the risk for inclusion of a female with an early undetected pregnancy

• Participants are stable non-smokers for at least 3 months preceding screening

• Other protocol defined inclusion criteria could apply.

Exclusion Criteria:

• History or presence of clinically relevant respiratory, gastrointestinal, renal, hepatic, hematological, lymphatic, neurological, cardiovascular, psychiatric, musculoskeletal, genitourinary, immunological, dermatological, connective tissue diseases or disorders.

• Prior history of cholecystectomy or splenectomy, and any clinically relevant surgery within 6 months prior to screening

• History of any malignancy

• History of chronic or recurrent acute infection or any bacterial, viral, parasitic or fungal infections within 30 days prior to screening and at any time between screening and admission, or hospitalization due to infection within 6 months prior to screening

• History of shingles within 12 months prior to screening

• History of drug hypersensitivity, ascertained or presumptive allergy/hypersensitivity to the active drug substance and/or formulation ingredients

• History of alcoholism or drug abuse within 2 years prior to screening, or evidence of such abuse as indicated by the laboratory assays conducted during screening

• History of residential exposure to tuberculosis, or a positive QuantiFERON® test within 4 weeks prior to screening

• Administration of live vaccines or live-attenuated virus vaccines within 3 months prior to screening

• Any condition, including findings in the laboratory tests, medical history, or other screening assessments, that in the opinion of the Investigator constitutes an inappropriate risk or a contraindication for participation in the study or that could interfere with the study's objectives, conduct, or evaluation

• Other protocol defined exclusion criteria could apply.

Related Conditions & MeSH terms

• Healthy

Intervention

Drug:
• Evobrutinib
Participants will receive single oral dose of evobrutinib either after an overnight fast of at least 10 hours (Treatment A and Treatment B), or under fed conditions that is within 30 minutes after start of high-fat meal (Treatment C) in period 1, 2 and 3.

Locations

Country	Name	City	State
Germany	Nuvisan GmbH	Neu-Ulm

Sponsors (1)

Lead Sponsor	Collaborator
Merck Healthcare KGaA, Darmstadt, Germany, an affiliate of Merck KGaA, Darmstadt, Germany

Country where clinical trial is conducted

Germany, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Area Under the Plasma Concentration-Time Curve From Time Zero to the Time of the Last Quantifiable Concentration (AUC0-t) of Evobrutinib Under Fasted Conditions		Pre-dose up to 24 hours post-dose on Day 6
Primary	Area Under the Plasma Concentration-Time Curve from Time Zero to Infinity (AUC0-inf) of Evobrutinib Under Fasted Conditions		Pre-dose up to 24 hours post-dose on Day 6
Primary	Maximum Observed Plasma Concentration (Cmax) of Evobrutinib Under Fasted Conditions		Pre-dose up to 24 hours post-dose on Day 6
Primary	Area Under the Plasma Concentration-Time Curve From Time Zero to the Time of the Last Quantifiable Concentration (AUC0-t) of Evobrutinib Under Fed Conditions		Pre-dose up to 24 hours post-dose on Day 6
Primary	Area Under the Plasma Concentration-Time Curve from Time Zero to Infinity (AUC0-inf) of Evobrutinib Under Fed Conditions		Pre-dose up to 24 hours post-dose on Day 6
Primary	Maximum Observed Plasma Concentration (Cmax) of Evobrutinib Under Fed Conditions		Pre-dose up to 24 hours post-dose on Day 6
Secondary	Number of Participants With Treatment -Emergent Adverse Events (TEAEs) Based on Severity Under Fasted Conditions		Day 1 up to Day 6
Secondary	Number of Participants With Clinically Significant Change From Baseline in Vital Signs, Laboratory Parameters and Electrocardiogram Findings Under Fasted Conditions	Number of participants with clinically significant change from baseline in vital signs, laboratory parameters and electrocardiogram findings will be reported	Day 1 up to Day 6
Secondary	Area Under the Plasma Concentration-Time Curve From Time Zero to Time 24 Hours After Evobrutinib Administration (AUC0-24)		Pre-dose up to 24 hours post-dose on Day 6
Secondary	Area Under The Plasma Concentration-Time Curve From Time Zero to Time 12 Hours After Evobrutinib Administration (AUC0-12)		Pre-dose up to 12 hours post-dose on Day 6
Secondary	Time to Reach Maximum Plasma Concentration (Tmax) of Evobrutinib		Pre-dose up to 24 hours post-dose on Day 6
Secondary	Time Prior to the First Measurable (non-zero) Concentration (t lag) of Evobrutinib		Pre-dose up to 24 hours post-dose on Day 6
Secondary	Terminal First Order (elimination) Rate Constant (?z) of Evobrutinib		Pre-dose up to 24 hours post-dose on Day 6
Secondary	Apparent Elimination Half Life (t1/2) of Evobrutinib		Pre-dose up to 24 hours post-dose on Day 6
Secondary	Apparent Total Body Clearance (CL/f) of Evobrutinib		Pre-dose up to 24 hours post-dose on Day 6
Secondary	Apparent Volume of Distribution During Terminal Phase (VZ/f) of Evobrutinib		Pre-dose up to 24 hours post-dose on Day 6
Secondary	Relative Bioavailability of Test Treatment in Relation to Reference Treatment (Frel)		Pre-dose up to 24 hours post-dose on Day 6

External Links

•   Trial Awareness and Transparency website