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Recruiting Phase 2, Phase 3 NCT07675980

NCT07675980 Thymosin-α1 for Recurrent Implantation Failure

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Clinical Trial Summary
NCT ID NCT07675980
Status Recruiting
Phase Phase 2, Phase 3
Sponsor Fakih IVF Fertility Center
Condition Recurrent Implantation Faliure
Study Type INTERVENTIONAL
Enrollment 136 participants
Start Date 2026-02-11
Primary Completion 2027-02

Eligibility & Interventions

Sex Female only
Min Age 18 Years
Max Age 40 Years
Study Type INTERVENTIONAL
Interventions
Thymosin Alpha1Placebo Control

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

In Phase 2, researchers evaluate early signs of effectiveness. You may be randomized to receive the active treatment or a comparator. Monitoring continues closely.

This trial targets 136 participants in total. It began in 2026-02-11 with a primary completion date of 2027-02.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Clinical trial evaluating the safety and efficacy of Thymosin-α1 (Tα1) as an adjunctive immunomodulatory therapy in women with unexplained recurrent implantation failure (RIF) undergoing IVF/ICSI cycles.

Eligibility Criteria

Inclusion Criteria: 1. -Women 18-40 years 2. -RIF- ≥2 failed embryo transfers with PGT-a tested euploid embryos 3. \- Normal parental karyotypes 4. \- Normal uterine cavity on imaging 5. \- Negative antiphospholipid panel 6. \- Thyroid and prolactin controlled within local reference standards Exclusion Criteria: 1. Identified/correctable non-immune cause of RPL (chromosomal, anatomic, endocrine) 2. \- Active malignancy 3. -Active infection 4. \- Uncontrolled systemic disease 5. \- Current systemic immunosuppression

Contact & Investigator

Central Contact

Dr. Lamiya Mohiyiddeen, MD, FRCOG

✉ lamiya.mohiyiddeen@fakihivf.com

📞 +971543676002

Principal Investigator

Dr. Michael Fakih, MD

PRINCIPAL INVESTIGATOR

Fakih IVF Abu Dhabi

Frequently Asked Questions

Who can join the NCT07675980 clinical trial?

This trial is open to female participants only, aged 18 Years or older, up to 40 Years, studying Recurrent Implantation Faliure. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

What phase is the NCT07675980 trial and what does that mean for participants?

Phase 2 trials evaluate whether the treatment shows signs of effectiveness while continuing to monitor safety. More participants are enrolled than in Phase 1 to help refine the treatment protocol.

Is NCT07675980 currently recruiting?

Yes, NCT07675980 is actively recruiting participants. Contact the research team at lamiya.mohiyiddeen@fakihivf.com for enrollment information.

Where is the NCT07675980 trial being conducted?

This trial is being conducted at Abu Dhabi, United Arab Emirates, Abu Dhabi, United Arab Emirates.

Who is sponsoring the NCT07675980 clinical trial?

NCT07675980 is sponsored by Fakih IVF Fertility Center. The principal investigator is Dr. Michael Fakih, MD at Fakih IVF Abu Dhabi. The trial plans to enroll 136 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: November 2026  ·  Data Methodology