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Clinical Trials/2025-524768-39-00
2025-524768-39-00RecruitingPhase 4

The pilot bioavailability study comparing the absorption of carbetocin (which is used as prevention of heavy bleeding after childbirth) in PABAL 100 μg/mL Solution for Injection when administered sublingually in the dose of 500 μg and intramuscularly in the dose of 100 μg.

Oxytone Bioscience B.V.1 site in 1 country4 target enrollmentStarted: February 9, 2026Last updated:
Conditions

Trial Snapshot

Phase
Phase 4
Status
Recruiting
Sponsor
Enrollment
4
Locations
1

Study Overview

Brief Summary

No summary available.

Eligibility Criteria

Ages
18 years to 64 years (18-64 Years)
Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Investigators

Sponsor
Oxytone Bioscience B.V.
Sponsor Class
Pharmaceutical company
Responsible Party
Principal Investigator
Principal Investigator

Yvone van Rijswick

Scientific

Oxytone Bioscience B.V.

Study Sites (1)

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