drugset / Trial / NCT07350317

Trial Comparing Subcutaneous Natural Progesterone (Prolutex) vs. Cetrorelix Acetate for Luteinizing Hormone Surge Suppression in Freeze-All IVF Cycles.

NCT07350317

Phase 4 Not yet recruiting 230 enrolled Trust Fertility Clinic
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The prevention of premature luteinizing hormone (LH) surge during controlled ovarian stimulation (COS) is critical for optimizing outcomes in assisted reproductive technology (ART). Cetrorelix acetate, a GnRH (Gonadotropin releasing hormone) antagonist administered subcutaneously, is the current standard for luteinizing hormone suppression. However, natural progesterone in a novel subcutaneous formulation (Prolutex) may offer a viable alternative. Prolutex is a water-soluble complex of natural progesterone with hydroxypropyl-β-cyclodextrin (HPBCD), patented as US Patent No. 4,727,064 Pitha, Jallowing for subcutaneous injection. This may simplify treatment and improve patient compliance. Progesterone forms are well studied and used globally/in UAE to suppress Luteinizing Hormone surge. It is an example of off-label use, which becomes a standard indication for use of progesterone. Several studies have demonstrated that exogenous progesterone can effectively suppress Luteinizing Hormone release while maintaining follicular development and oocyte competence. Furthermore, progestin-based protocols are potentially more cost-effective and similar to administer compared to GnRH (Gonadotropin releasing hormone) antagonists. To our knowledge, this is the first randomized trial directly comparing a subcutaneous progesterone formulation (Prolutex) with cetrorelix acetate, administered via the same route, in terms of luteinizing hormone surge suppression. For this specific research, there are no relevant published studies available. This Randomised controlled trial will be done to address the research gap and compare the two already approved standard of care medications to see if Prolutex can be used as a viable alternative to suppress Luteinizing Hormone levels.

Timeline

Start
2026-01
Primary completion
2026-12
Completion
2027-02

Publications

  • Background 1. Griesinger G, et al. Reprod Biol Endocrinol. 2016;14(1):29 2. Fatemi HM, et al. Hum Reprod. 2019;34(7):1223-34 3. Vuong LN, et al. Fertil Steril. 2021;116(5):1148-57 4. Papanikolaou EG, et al. J Assist Reprod Genet. 2020;37(4):841-50 5. Pitha J. US Patent No. 4,727,064

Drugs

EvaluationDrugModalityDoseRoute
Subject Cetrorelix Other / unclassified 0.25 mg Subcutaneous
Subject Progesterone Other / unclassified 25 mg Subcutaneous

Indications

No indication recorded.