Usefulness of Corifollitropin α as Alternative to Conventional Daily rFSH Protocols in Oocyte Donors Undergoing Pituitary Suppression With Medroxiprogesterona Acetate (MPA)

Infertility, Female Clinical Trial

— TROPIX  

Official title:

Usefulness of Corifollitropin α as Alternative to Conventional Daily rFSH Protocols in Oocyte Donors Undergoing Pituitary Suppression With Medroxiprogesterona Acetate (MPA)

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT06193135
• Other study ID #: 2304-VLC-051-JG
• Status: Not yet recruiting
• Phase: N/A
• Start date: March 1, 2024
• Est. completion date: December 31, 2025

Study information

• Verified date: January 2024
• Source: Instituto Valenciano de Infertilidad, IVI VALENCIA
• Contact: JUAN GILES, PhD
• Phone: +34 963.05.90.00
• Email: juan.giles[@]ivirma.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

IVF patients frequently experience physical, emotional or physicological burden; this is particularly relevant in the case of oocyte donors, since young women undergo a procedure that is of no health benefit to them. One of the phases of the treatment that contributes most to this situation is ovarian stimulation; as it involves the administration of daily injections which, in addition to the discomfort of administration, causes anxiety to the patient about its correct administration and possible side effects and to physicians concerns about patient compliance.

Advances in pharmacology and knowledge of ovarian pathophysiology have led to the development of new protocols that simplify and reduce drug administration, decrease the potential risk of misapplication and contribute to an improved patient experience. In this context, Corifollitropin α, a long-acting recombinant FSH (rFSH) molecule, provides with a single subcutaneous injection similar results as daily administration of rFSH during a week.

On the other hand, conventional stimulation protocols used in ART resort to using a GnRH analogue (agonist or antagonist) to prevent early luteinization, which is defined as the presence of a progesterone value of > 1.5 ng/ml on the day of induced ovulation. Nevertheless, its use presents some disadvantages, such as it being sometimes complex to achieve desensitization or consistent hypothalamic block, risk of OHS when ovulation is triggered with HCG or its cost. Hence the interest in exploring new options to prevent a premature peak in LH. Nowadays, the oral administration of progestagens (progesterone-primed ovarian stimulation [PPOS]) during the follicular phase of ovarian stimulation (OS) has emerged as an attractive alternative to conventional protocols for preventing early luteinization. Moreover, PPOS produces a similar or even better, in some subgroups, response to OS (length of treatment, number of MII, cancelation rate, etc.), reproductive outcomes (pregnancy rate, live birth rate, etc) and safety (rate of ovarian hyperstimulation [OHSS] or congenital malformations).

Thus, PPOS would seem to be an effective option for personalized protocols, particularly when fresh embryo transfer (FET) is not to be performed, a circumstance that is likely to rise in frequency given the progressive increase in women's age at childbearing; for example, in oocyte donation, or in fertility preservation (FP) and preimplantation genetic testing for aneuploidy (PGT-A). However, very little data are available regarding cycle outcome following Corifollitropin α and PPOS as pituitary suppressor.

The present study, a prospective RCT, was designed to evaluate cycle characteristics (MII oocytes as the primary objective) and endocrinologic profiles of oocyte donors receiving Corifollitropin α and MPA as co-treatment compared with those receiving a daily dose of rFSH (follitropin β) as a control.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 318
• Est. completion date: December 31, 2025
• Est. primary completion date: December 31, 2025
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years to 35 Years

Eligibility

Inclusion Criteria:

• Signature of the subject's informed consent prior to any trial-related activity.

• Age between 18 and 35 years (both inclusive).

• Regular menstrual cycle, from 25 to 35 days (both inclusive).

• Absence of physical and psychological illness at the time of donation at the discretion of the investigator.

• BMI 18-28 kg/m2 (both inclusive) at the time of donation.

• No personal or family history of interest at the discretion of the investigator.

• Normal uterus and ovaries, without organic pathology.

• No polycystic ovaries.

• Antral follicle count greater than 12 in the sum of the two ovaries at the time of the screening visit.

• Normal karyotype.

• Negative infectious disease screening (Hepatitis B Virus, Hepatitis C Virus, Human Immunodeficiency Virus and Syphilis).

• General analysis with hemogram, hemostasis and biochemistry with parameters within normality.

Exclusion Criteria:

• Concurrent participation in another clinical trial.

• Previous participation in this clinical trial.

• Use of long-term hormonal contraception (hormonal IUD or subcutaneous implants) at least 1 month prior to enrollment.

• Any systemic or metabolic disorder (i.e.: diabetes...) that contraindicates the use of gonadotropins.

• Personal history of thrombophlebitis and thromboembolic phenomena and hypertension.

• Severe hepatic insufficiency, cardiovascular disease

• Suspicion or evidence of breast malignancy or hormone-dependent genital organs.

• Known hypersensitivity to AMP or its excipients

• Any reason for exclusion from the oocyte donation program.

Related Conditions & MeSH terms

• Infertility
• Infertility, Female
• Reproductive Sterility

Intervention

Drug:
• Corifolitropin Alfa
Patients will receive a single dose of Colifolitropin alfa, then will receive daily dose of Folitropin Beta since triggering criteria are met.
• Folitropin Beta
Patient will receive daily dose of Folitropin Beta since triggering criteria are met.

Locations

Country	Name	City	State
Spain	IVI Valencia	Valencia

Sponsors (1)

Lead Sponsor	Collaborator
Instituto Valenciano de Infertilidad, IVI VALENCIA

Country where clinical trial is conducted

Spain, 

References & Publications (4)

Boostanfar R, Shapiro B, Levy M, Rosenwaks Z, Witjes H, Stegmann BJ, Elbers J, Gordon K, Mannaerts B; Pursue investigators. Large, comparative, randomized double-blind trial confirming noninferiority of pregnancy rates for corifollitropin alfa compared wi — View Citation

Corifollitropin alfa Ensure Study Group. Corifollitropin alfa for ovarian stimulation in IVF: a randomized trial in lower-body-weight women. Reprod Biomed Online. 2010 Jul;21(1):66-76. doi: 10.1016/j.rbmo.2010.03.019. Epub 2010 Mar 28. Erratum In: Reprod — View Citation

Kalfoglou AL. Navigating conflict of interest in oocyte donation. Am J Bioeth. 2001 Fall;1(4):W1. doi: 10.1162/152651601317139333. No abstract available. — View Citation

Requena A, Cruz M, Collado D, Izquierdo A, Ballesteros A, Munoz M, Garcia-Velasco JA. Evaluation of the degree of satisfaction in oocyte donors using sustained-release FSH corifollitropin alpha. Reprod Biomed Online. 2013 Mar;26(3):253-9. doi: 10.1016/j.r — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	To compare the number of total oocytes obtained after controlled ovarian stimulation with a-Corifolitropin vs. ß-Folitropin in donors in whom medroxyprogesterone acetate (MPA) was used to prevent early luteinization.	Number of total oocytes and oocytes metaphase II	2 years
Primary	To compare the number of metaphase II (MII) oocytes obtained after controlled ovarian stimulation with a-Corifolitropin vs. ß-Folitropin in donors in whom medroxyprogesterone acetate (MPA) was used to prevent early luteinization.	Quantification of total oocytes in metaphase II	2 years
Secondary	Incidence of early luteinization	Quantification of cycle cancellation due to lack of response and failure to obtain MII oocytes in puncture.	2 years
Secondary	Medication tolerance: pain, abdominal distension, ovarian hyperstimulation syndrome (OHSS), etc.	Quantification of pain, abdominal distension, ovarian hyperstimulation syndrome (OHSS) using a specifically designed questionarie for this strudy.	2 years
Secondary	Controlled ovraian stimulation duration	Quantification of total days of estimulation	2 years
Secondary	Total cost of each stimulation type.	Quantification of cost.	2 years