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Clinical Trials/NL-OMON45496
NL-OMON45496
Completed
Not Applicable

A phase 1, randomized, placebo-controlled study to assess the safety and pharmacokinetics of multiple ascending dose regimens of TP-6076. - TP-6076 MAD study

Tetraphase Pharmaceuticals, Inc.0 sites56 target enrollmentTBD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Infecties.
Sponsor
Tetraphase Pharmaceuticals, Inc.
Enrollment
56
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Eligibility Criteria

Inclusion Criteria

  • Healthy male or female
  • 18\-55 years, inclusive
  • BMI 18\.0\-35\.0 kilogram/meter2
  • Weight between 50 (female) and 60 (male) and 105 kilograms, inclusive
  • Non smokers

Exclusion Criteria

  • Suffering from hepatitis B, hepatitis C, cancer or HIV/AIDS. In case of participation in another drug study within 90 days before the start of this study or being a blood donor within 60 days from the start of the study. In case of donating more than 1\.5 liters of blood in the 10 months prior the start of this study.

Outcomes

Primary Outcomes

Not specified

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