Drug · CHEMBL103
PROGESTERONE
7 sourcespipelines-2026-09-18-0.3.1
Cite this record
ConductScience Library. PROGESTERONE. Drugs and targets, record CHEMBL103. Release pipelines-2026-09-18-0.3.1, 18 Sept 2026. https://conductscience.org/library/drugs/CHEMBL103
On this page
Drug
Names and IDs as ChEMBL gives them, through Open Targets.
- Brand names
Crinone, Cyclogest, Endometrin, Lutigest, Milprosa, Prochieve, Progesta-care, Progestasert, Progesterone component of bijuva, Progestin, Prometrium, Regumate, Serenity for women, Syngestrone, Utrogestan
- ChEMBL
- Open Targets' highest stage
- Approval, for 4 of its 69 diseases, from DailyMed, PMDA and TTD
- Open Targets
Targets1
The targets ChEMBL's mechanism records give for the drug, through Open Targets. A mechanism record says what the drug acts on, not how strongly.
| Target | Protein | Mechanism | Action | Gene in Genes |
|---|---|---|---|---|
| PGR | Progesterone receptor | Progesterone receptor agonist | AGONIST | https://conductscience.org/library/genes/5241 |
Source ChEMBL
Diseases69
The diseases Open Targets' clinical reports study the drug for, the most trial reports first. The stage is Open Targets', the highest any of its sources reports for the pair, and each row names the sources that report it.
1 to 10 of 69Source Open Targets
See all 69 diseasesTrials421
Trials whose record names the drug by a name ChEMBL states, posted results first, then the largest. Open Targets read each trial's text to find its drugs. 3 more rest on that reading alone and are shown because the trials' posted result groups or NLM's indexing of their papers name the drug. 9 more that Open Targets linked to it are not shown, since the release's checks do not confirm them.
| Trial | Title | Phase | Participants | Results first posted | Named as | Linked by | Source |
|---|---|---|---|---|---|---|---|
| NCT01942668 | A Safety and Efficacy Study of the Combination Estradiol and Progesterone to Treat Vasomotor Symptoms | Phase 3 | 1,845 | 2019-05-06 | progesterone | Its name | ClinicalTrials.gov |
| NCT02518594 | A Trial of Pessary and Progesterone for Preterm Prevention in Twin Gestation With a Short Cervix | Phase 3 | 1,311 | 2026-03-10 | progesterone | Its name | ClinicalTrials.gov |
| NCT01143064 | Efficacy and Safety Study of Intravenous Progesterone in Patients With Severe Traumatic Brain Injury | Phase 3 | 1,195 | 2024-10-02 | progesterone | Its name | ClinicalTrials.gov |
| NCT01850030 | A Multicenter Study Comparing the Efficacy, Safety and Tolerability of Oral Dydrogesterone 30 mg Daily Versus Intravaginal Micronized Progesterone Capsules 600 mg Daily for Luteal Support in In-Vitro Fertilization | Phase 3 | 1,070 | 2018-01-02 | progesterone | Its name | ClinicalTrials.gov |
| NCT02491437 | A Study Comparing the Efficacy, Safety and Tolerability of Oral Dydrogesterone 30 mg Daily Versus Crinone 8% Intravaginal Progesterone Gel 90 mg Daily for Luteal Support in In-Vitro Fertilization (LOTUS II) | Phase 3 | 1,034 | 2019-10-01 | progesterone | Its name | ClinicalTrials.gov |
| NCT00822900 | Progesterone for the Treatment of Traumatic Brain Injury III | Phase 3 | 882 | 2015-07-03 | progesterone | Its name | ClinicalTrials.gov |
| NCT00828191 | Subcutaneous Progesterone Versus Vaginal Progesterone Tablets for Luteal Phase Support in In Vitro Fertilization (IVF) | Phase 3 | 800 | 2012-12-26 | progesterone | Its name | ClinicalTrials.gov |
| NCT00827983 | Subcutaneous Progesterone Versus Vaginal Progesterone Gel for Luteal Phase Support in Patients Undergoing In-Vitro Fertilization (IVF) | Phase 3 | 683 | 2012-12-26 | progesterone | Its name | ClinicalTrials.gov |
| NCT02524561 | KEEPS Mammographic Density And Breast Health Ancillary Study | 517 | 2017-03-08 | progesterone | Its name | ClinicalTrials.gov | |
| NCT00656201 | Comparison of Crinone 8% Intravaginal Gel and IM Progesterone Supplementation for In Vitro Fertilization (IVF) | Phase 4 | 468 | 2011-09-20 | progesterone | Its name | ClinicalTrials.gov |
1 to 10 of 421
See all 421 trialsComparisons in its trials135
Comparisons Trial comparisons calculated in the trials whose record names the drug, most participants first. A comparison in one of its trials does not always compare the drug, so read the two groups.
| Comparison | Group 1, with the outcome | Group 2, with the outcome | Participants | Trial | Source |
|---|---|---|---|---|---|
| BHR-100 vs Placebo: deaths from any cause | 109 of 596 | 95 of 583 | 1,179 | NCT01143064 | Trial comparisons |
| BHR-100 vs Placebo: serious adverse events | 224 of 596 | 214 of 583 | 1,179 | NCT01143064 | Trial comparisons |
| Dydrogesterone 30 mg vs Micronized Progesterone 600 mg: serious adverse events | 56 of 518 | 68 of 511 | 1,029 | NCT01850030 | Trial comparisons |
| Progesterone vs Placebo: serious adverse events | 246 of 442 | 251 of 440 | 882 | NCT00822900 | Trial comparisons |
| Progesterone SC vs Progesterone Tablets: serious adverse events | 0 of 400 | 0 of 400 | 800 | NCT00828191 | Trial comparisons |
| Progesterone SC vs Progesterone Vaginal Gel: serious adverse events | 14 of 338 | 20 of 344 | 682 | NCT00827983 | Trial comparisons |
| Expectant Mothers - Corifollitropin Alfa 150 µg vs Fetuses Present at 10 Weeks After Fresh ET in Base Study: serious adverse events | 145 of 268 | 84 of 315 | 583 | NCT00702234 | Trial comparisons |
| Prochieve vs Placebo: serious adverse events | 97 of 235 | 98 of 224 | 459 | NCT00615550 | Trial comparisons |
| Prochieve vs Placebo: Number of Neonates Who Died. | 3 of 235 | 5 of 223 | 458 | NCT00615550 | Trial comparisons |
| Prochieve vs Placebo: Number of Participants With Birth <=32 6/7 Weeks Gestation. | 21 of 235 | 36 of 223 | 458 | NCT00615550 | Trial comparisons |
1 to 10 of 135
See all 135 comparisons in its trialsPapers from its trials267
The papers the trials whose record names the drug list on ClinicalTrials.gov as their results (RESULT) or as drawn from them (DERIVED), results first, newest first.
Tests in its trials10
The tests ConductCognition runs that the trials whose record names the drug name in their registered outcomes, as ScienceGraph matched them. ConductCognition's list names the tests it runs, not every test a trial used.
| Test | Trials naming it as an outcome | As a primary outcome | Source |
|---|---|---|---|
| Monetary Incentive Delay | 3 | 3 | ConductCognition |
| Dot-Probe Task | 2 | 1 | ConductCognition |
| Go/No-Go Task | 2 | 1 | ConductCognition |
| Point Subtraction Aggression Task | 2 | 1 | ConductCognition |
| Posner Cueing | 2 | 1 | ConductCognition |
| Verbal Learning | 2 | 0 | ConductCognition |
| Delay Discounting | 1 | 1 | ConductCognition |
| Effort for Rewards Task | 1 | 0 | ConductCognition |
| Stroop Color-Word Test | 1 | 0 | ConductCognition |
| Symbol Coding | 1 | 0 | ConductCognition |
Data dates
The date of each source this release read.
Sources 7
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ChEMBL, through Open TargetsCC BY-SA 3.0
- ConductCognition's list of its testsOur own data
- ClinicalTrials.govNo license stated
- NLM's MeSHNLM's terms
- Open TargetsCC0 1.0
- PubMedNLM's terms
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
- ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
- ConductCognition's list of its testsOur own data: ConductCognition's list of its tests, https://conductcognition.com
- ClinicalTrials.govnone stated
- NLM's MeSHNLM's
- Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
- PubMedNLM's terms
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this drug from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/drugs/v1/CHEMBL103
GET https://conductscience.org/api/drugs/v1/CHEMBL103/diseases?page=2