# The Molecular Basis of Inherited Reproductive Disorders

> **NCT05971836** · — · ACTIVE_NOT_RECRUITING · sponsor: **Stephanie B. Seminara, MD** · enrollment: 600 (estimated)

## Conditions studied

- Hypogonadotropic Hypogonadism
- Reproductive Disorder
- Kallmann Syndrome
- Delayed Puberty

## Interventions

_None listed._

## Key facts

- **NCT ID:** NCT05971836
- **Lead sponsor:** Stephanie B. Seminara, MD
- **Sponsor class:** OTHER
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** ACTIVE_NOT_RECRUITING
- **Start date:** 2021-01-21
- **Primary completion:** 2027-03
- **Final completion:** 2027-03
- **Target enrollment:** 600 (ESTIMATED)
- **Last updated:** 2026-04-15


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT05971836

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT05971836, "The Molecular Basis of Inherited Reproductive Disorders". Retrieved via AI Analytics 2026-06-08 from https://api.ai-analytics.org/clinical/NCT05971836. Licensed CC0.

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*[Clinical trials dataset](/datasets/clinical-trials) · CC0 1.0*