Coadministration of the prostaglandin F2α receptor antagonist preterm labour drug candidate OBE022 with magnesium sulfate, atosiban, nifedipine and betamethasone

Br J Clin Pharmacol. 2019 Jul;85(7):1516-1527. doi: 10.1111/bcp.13925. Epub 2019 May 11.

Abstract

Aims: To investigate presence or absence of clinically relevant drug interactions (pharmacokinetic and safety/tolerability) of OBE022 with standard-of-care medicines for preterm labour, enabling coadministration and further clinical development.

Methods: Part A: open-label, randomized, 3-period crossover assessing coadministration of single doses of OBE022 (1100 mg) and MgSO4 . Part B: open-label, single-sequence crossover assessing the interactions following administration of OBE022 (1000 mg/day) at steady state coadministered with single doses of atosiban, nifedipine and betamethasone. Twenty-five healthy nonpregnant women of reproductive age were enrolled (Part A: n = 12; Part B: n = 13).

Results: OBE022, alone or in combination with standard-of-care medications, was well tolerated. Headache and dizziness were the most frequently reported adverse events; dizziness occurred more often with the nifedipine/OBE022 combination. There were no clinically significant pharmacokinetic interactions when coadministered with MgSO4 . Co-administration had no notable effect on atosiban exposure. Atosiban reduced exposure to OBE002 (peak concentration [Cmax ] 22%, area under the concentration-time curve [AUC] 19%). Coadministration with betamethasone slightly increased betamethasone exposure (Cmax + 18%, AUC +27%) and OBE002 exposure (Cmax + 35%, AUC +15%). These changes were not considered clinically significant. Coadministration with nifedipine slightly increased OBE002 exposure (Cmax + 29%, AUC +24%) and markedly increased nifedipine exposure (Cmax by 2-fold and AUC by 2-fold), which may be clinically significant.

Conclusions: The use of OBE022, a PGF2α antagonist prodrug, in combination with standard-of-care medicines may provide new treatment alternatives for preterm labour. All tested combinations were well tolerated. Nifedipine doses could potentially be reduced or staggered when coadministered with OBE022.

Keywords: OBE022; drug-drug interaction; pharmacokinetics; safety; tocolytic.

Publication types

  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Area Under Curve
  • Betamethasone / administration & dosage
  • Betamethasone / pharmacology
  • Cross-Over Studies
  • Drug Interactions
  • Esters / administration & dosage*
  • Esters / adverse effects
  • Esters / pharmacokinetics
  • Female
  • Humans
  • Magnesium Sulfate / administration & dosage
  • Magnesium Sulfate / pharmacology
  • Middle Aged
  • Nifedipine / administration & dosage
  • Nifedipine / pharmacology
  • Receptors, Prostaglandin / antagonists & inhibitors
  • Sulfones / administration & dosage*
  • Sulfones / adverse effects
  • Sulfones / pharmacokinetics
  • Thiazolidines / administration & dosage*
  • Thiazolidines / adverse effects
  • Thiazolidines / pharmacokinetics
  • Tocolytic Agents / administration & dosage*
  • Tocolytic Agents / adverse effects
  • Tocolytic Agents / pharmacokinetics
  • Vasotocin / administration & dosage
  • Vasotocin / analogs & derivatives
  • Vasotocin / pharmacology
  • Young Adult

Substances

  • Esters
  • Receptors, Prostaglandin
  • Sulfones
  • Thiazolidines
  • Tocolytic Agents
  • obe022
  • prostaglandin F2alpha receptor
  • atosiban
  • Magnesium Sulfate
  • Betamethasone
  • Nifedipine
  • Vasotocin