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A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Proof of Concept Study (section A) with a conditional dose finding follow up (Section B) to Evaluate the Efficacy on Cervical ripening, Safety, Tolerability and dose response of Subcutaneously Administered Tafoxiparin in Term Pregnant, Nulliparous Women with an unripe cervix undergoing Labor Induction

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Trial Profile

A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Proof of Concept Study (section A) with a conditional dose finding follow up (Section B) to Evaluate the Efficacy on Cervical ripening, Safety, Tolerability and dose response of Subcutaneously Administered Tafoxiparin in Term Pregnant, Nulliparous Women with an unripe cervix undergoing Labor Induction

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 14 Apr 2025

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At a glance

  • Drugs Tafoxiparin (Primary)
  • Indications Labour disorders; Labour induction
  • Focus Proof of concept; Therapeutic Use
  • Sponsors Dilafor

Most Recent Events

  • 30 Mar 2023 Status changed from active, no longer recruiting to completed.
  • 15 Mar 2023 This trial has been completed in Sweden (2022-12-30), according to European Clinical Trials Database record.
  • 27 Dec 2022 According to a Karolinska Development media release, the company has enrolled the last patient to the extension phase of the trial. The results are expected to be presented in the first quarter of 2023.

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