A Randomised, Phase II, Comparative Study With a Parallel Control for Evaluating the Efficacy and Safety of Combined Treatment of Lutropin Alpha and Recombinant Human Luteinizing Hormone in the Middle of the Controlled Ovarian Stimulation Follicular Phase in Women With Reduced Ovarian Reserve

Merck KGaA (EMD Serono)

Status and phase

Completed

Phase 2

Conditions

Infertility

Ovulation Induction

Treatments

Drug: Recombinant human follicle stimulating hormone (r-hFSH)

Drug: Recombinant human luteinizing hormone (r-hLH)

Study type

Interventional

Funder types

Industry

Identifiers

NCT01110707

IMP 25186

Details and patient eligibility

About

This was a prospective, randomized, Phase II, comparative study with a parallel control for evaluating the efficacy and safety of combined treatment of recombinant human follicle stimulating hormone (r-hFSH) and recombinant human luteinizing hormone (r-hLH). The combined treatment was administered at the middle of the follicular phase in subjects undergoing in-vitro fertilisation (IVF) through intracytoplasmic sperm injection (ICSI) and transfer of embryos (ET).

Enrollment

131 patients

Sex

Female

Ages

35 to 40 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

All subjects must meet the following inclusion criteria within the 6 months prior to starting the pituitary suppression unless otherwise specified:

Postmenopausal woman aged between 35 and 40 years that wishes to become pregnant
Subjects with basal serum level (beginning of the follicular phase, Day 2-5) of Follicle-Stimulating Hormone (FSH) less than 10 IU/L determined within the 6 months prior as well as Luteinizing hormone (LH) and Estradiol (E2) levels within the normal interval according to standard data for the area where the study was carried out
Subjects with a regular menstrual cycles between 25-35 days
Subjects with infertility that justifies treatment with IVF/ET or ICSI
Subjects undergoing controlled ovarian stimulation (COS) with r-hFSH using a long protocol with GnRH-a
Sperm availability from the subject's current partner unless it is planned to use sperm from a donor
Subjects with both ovaries
Subjects with uterine cavity capable of withstanding the implantation of the embryo and pregnancy
Subjects whose vaginal smear (PAP) was normal within the 3 years prior to starting the stimulation
Subjects with body mass index (BMI) between 18 and 30 at the time of participation in the study
Subjects in whom at least 30 days have elapsed since the last dose of clomiphene citrate or gonadotropins before beginning treatment with GnRH-a
Subjects with a negative pregnancy test result using the beta human chorionic gonadotropin (beta-hCG) test (in urine or blood) before beginning treatment with GnRH-a
Subjects willing to and capable of following the protocol during the entire study
Subjects who have provided informed written consent before carrying out any procedure related with the study (that is not part of the normal medical treatment followed by the subject)

Exclusion criteria

Subject who were human immunodeficiency virus, hepatitis B and C virus positive
Subjects suffering from any clinically important systematic disease, hypothalmic or pituitary tumour, ovarian, uterine or breast cancer, endocrinopathy and/or medical alterations, biochemical or hematological that as per the investigators judgement, may interfere with the gonadotropin treatment
Subjects who have been subjected to more than 2 assisted reproductive cycles in the past
Subjects who have cancelled 2 cycles in the past
Subjects who have cryopreserved embryos from previous assisted reproductive cycles
Subjects with non explained vaginal haemorrhages
Subjects with polycystic ovary, enlarged ovary or ovarian cysts of unknown aetiology
Subjects with any contraindication for getting pregnant or taking the pregnancy to full term
Subjects with known allergy to the gonadotropin preparations or any of its excipients
Subjects with current drug use or prior personal history of alcohol, drug or psychiatric drug dependency in the past five years
Subjects with prior participation in this study or simultaneous participation in a different clinical study with a medication under investigation
Subjects who were not willing to or incapable of following the study protocol