Trial · NCT07216742
Human Menopausal Gonadotropin Research in Infertility Assessing Cumulative Live Birth With Frozen Embryo Transfer.
NCT07216742, Phase 3, Active not recruiting, Granata Bio Corporation
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Human Menopausal Gonadotropin Research in Infertility Assessing Cumulative Live Birth With Frozen Embryo Transfer. Trials, record NCT07216742. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07216742
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Human Menopausal Gonadotropin Research in Infertility Assessing Cumulative Live Birth With Frozen Embryo Transfer.
- NCT number
- NCT07216742
- Status
- Active not recruiting
- Phases
- Phase 3
- Enrollment
- 659 participants, estimated
- Lead sponsor
- Granata Bio Corporation
- Conditions
- Infertility (IVF Patients)
- Interventions
- hMG subcutaneous injection, Placebo
- First posted
- 2025-10-15
- Last updated
- 2026-11-05
Source ClinicalTrials.gov
Registered outcomes41
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | cumulative live birth rate | 12 months | cumulative live birth rate following vitrified-thawed, single-euploid blastocyst transfer(s) |
| Secondary | Positive pregnancy (serum β-human chorionic gonadotropin [hCG]) | 10 +/-2 days after Embryo transfer | |
| Secondary | Clinical pregnancy (intrauterine gestational sac with fetal heartbeat) | 5 weeks ± 6 days post-embryo transfer | |
| Secondary | Ongoing pregnancy (intrauterine pregnancy with fetal heartbeat) | 10 weeks ± 6 days post-embryo transfer (ET) | |
| Secondary | Live birth rate | 9 months after ET | |
| Secondary | Number of oocytes retrieved per stimulation cycle | 12-22 days after controlled ovarian stimulation start | |
| Secondary | Number of metaphase II (MII) oocytes retrieved | 12-22 days after controlled ovarian stimulation start | |
| Secondary | Fertilization rate (proportion of MII oocytes with normal fertilization) | 12-22 days after Controlled Ovarian stimulation start | |
| Secondary | Number of Day 5 blastocysts from oocyte retrievals from Period 1 and Period 2 | 12-22 days after controlled ovarian stimulation start | |
| Secondary | Total gonadotropin dose required per stimulation cycle | 12-20 days after start Controlled ovarian stimulation |
1 to 10 of 41Source ClinicalTrials.gov
See all 41 registered outcomesOutcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07216742
GET https://conductscience.org/api/trials/v1/NCT07216742/registered?page=2