Actively Recruiting

Phase 3
Age: 18Years - 40Years
FEMALE
NCT05930613

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

Age: 18Years - 40Years
FEMALE

Eligibility Criteria

Eligible

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
Not Eligible

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

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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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