Actively Recruiting
Certolizumab in Recurrent Implantation Failure (RIF)
Led by Assistance Publique - Hôpitaux de Paris · Updated on 2023-12-11
161
Participants Needed
1
Research Sites
278 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Recurrent implantation failure (RIF), defined as the absence of clinical pregnancy after the transfer of three good-quality embryos, concerns up to 40% of IVF couples and is associated with a low success rate. The causes remain unexplained in over 50% of cases. Various dysimmune changes (related to immune T cells profiles, pro-inflammatory cytokines levels) have been described in unexplained RIF as compared to fertile controls, and it has been estimated that such dysimmunity may occur in 50% of unexplained RIFs. Previous data on a benefit of general immune modulation by steroids or immunoglobulins are heterogenous and failed to demonstrate clinically significant benefit. The proinflammatory cytokine Tumor Necrosis Factor (TNF) α participates in the regulation of the immune balance of the endometrium, its peripheral blood and endometrial concentrations are increased in RIF patients as compared to fertile controls. In 2009, a pilot placebo controlled study showed that TNF-α antagonist treatment allowed a 56% live birth rate (versus 13% in controls) in 13 women with unexplained RIF. Due to the lack of maternal and fetal tolerance data, TNF-α antagonists were not further evaluated. Today, safety data issued from 1200 pregnancies are reassuring allowing the use of TNF-α antagonists during pregnancy (www.lecrat.org). In addition the TNF-α antagonist certolizumab does not cross the placental barrier. We hypothesize that certolizumab may improve clinical pregnancy rates in women with unexplained RIF with a good safety profile.
CONDITIONS
Official Title
Certolizumab in Recurrent Implantation Failure (RIF)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Women aged 18-40 years
- Idiopathic, male or tubal factor infertility
- Unexplained recurrent implantation failure defined as failure to achieve clinical pregnancy after at least three transfers of good-quality embryos (Istanbul criteria)
- Affiliation to a French social security system (beneficiary or legal)
- Informed and signed consent
You will not qualify if you...
- Known causes of recurrent implantation failure, including genetic parental anomalies
- Type I or II non-gestational diabetes mellitus
- Infectious diseases
- Antiphospholipid syndrome
- Sickle cell disease
- Diffuse adenomyosis
- Contraindication to freeze-thaw embryo transfer (FET) treatment
- Hypersensitivity to certolizumab or any excipients
- Primary or secondary immunodeficiency
- Active uncontrolled infections or active tuberculosis
- Moderate to severe cardiac insufficiency (NYHA III/IV)
- Any malignant neoplasm except adequately treated basal or squamous cell carcinoma of the skin
- Immunization with live or attenuated vaccine within 4 weeks prior to baseline or during treatment
- Cytopenia as defined by specified low blood counts
- Liver cytolysis with AST/ALT greater than 5 times normal
- Insufficient kidney function with serum creatinine over 3 mg/dL or creatinine clearance 20 ml/min or less
- Demyelinating neurological disease
- Hypersensitivity to rifampicin and isoniazid or related excipients
- Porphyria
- Decreased blood clotting from low vitamin K
- Combination with specified drugs
- Acute hepatitis, hepatic failure, or chronic liver disease
- Acute nephropathy
- Contraindication to anti-pneumococcal vaccination
- Absence of health insurance
- Subject under guardianship or curatorship
- Subject deprived of liberty by judicial or administrative decision
- Participation in another interventional study or within exclusion period
AI-Screening
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Trial Site Locations
Total: 1 location
1
Saint-Antoine Hospital - APHP
Paris, France, 75012
Actively Recruiting
Research Team
N
Nathalie CHABBERT-BUFFET, Pr
CONTACT
K
KOLANSKA Kamila, Dr
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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