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A Study of RO6926496 in Healthy Volunteers

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Roche

Status and phase

Completed
Phase 1

Conditions

Healthy Volunteer

Treatments

Drug: Placebo
Drug: RO6926496

Study type

Interventional

Funder types

Industry

Identifiers

NCT02281786
2014-003170-16 (EudraCT Number)
BP29462

Details and patient eligibility

About

This is a single center, randomized, investigator/subject blind, single ascending dose, placebo-controlled, parallel study that will evaluate the safety, tolerability and pharmacokinetics of RO6926496 in healthy male participants. The dose escalation is adaptive in nature. It is planned to enroll 48 subjects in 6 cohorts. The anticipated total duration of the study is 16 weeks.

Enrollment

48 patients

Sex

Male

Ages

18 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Healthy male participants, 18 to 45 years of age; healthy status is defined by absence of evidence of any active or chronic disease following a detailed medical and surgical history
  • A body mass index between 18 and 30 kg/m2
  • Male subjects and their partners of childbearing potential must agree to use 2 methods of contraception, one of which must be a barrier method for the duration of the study

Exclusion criteria

  • Positive hepatitis B, hepatitis C, or HIV infection
  • History of any clinically significant disease or disorder
  • Clinically significant abnormalities in laboratory test results
  • Participation in an investigational drug or device study within 90 days prior to screening
  • Concomitant disease or condition that could interfere with, or treatment of which might interfere with, the conduct of the study, or that would, in the opinion of the investigator, pose an unacceptable risk to the subject in this study
  • History or presence of clinically significant ECG abnormalities
  • Smokers who smoke more than 10 cigarettes daily or equivalent and unable or unwilling not to smoke during the in-clinic period
  • Any clinically relevant history of hypersensitivity or allergic reactions
  • Any familial history of early onset Alzheimer's disease

Trial design

48 participants in 6 patient groups

Cohort 1
Experimental group
Description:
8 volunteers (6 active, 2 placebo)
Treatment:
Drug: RO6926496
Drug: Placebo
Cohort 2
Experimental group
Description:
8 volunteers (6 active, 2 placebo)
Treatment:
Drug: RO6926496
Drug: Placebo
Cohort 3
Experimental group
Description:
8 volunteers (6 active, 2 placebo)
Treatment:
Drug: RO6926496
Drug: Placebo
Cohort 4
Experimental group
Description:
8 volunteers (6 active, 2 placebo)
Treatment:
Drug: RO6926496
Drug: Placebo
Cohort 5
Experimental group
Description:
8 volunteers (6 active, 2 placebo)
Treatment:
Drug: RO6926496
Drug: Placebo
Cohort 6
Experimental group
Description:
8 volunteers (6 active, 2 placebo)
Treatment:
Drug: RO6926496
Drug: Placebo

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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