Overview
Human chorionic gonadotropin (HCG), a polypeptide hormone produced by the human placenta. Endogenously produced HCG interacts with the LHCG receptor of the ovary and promotes the maintenance of the corpus luteum during the beginning of pregnancy. This allows the corpus luteum to continuously secrete the hormone progesterone during the first trimester, which is required for maintenance of the uterus and prevents menstruation. In males, HCG also stimulates the production of gonadal steroid hormones by stimulating the interstitial cells (Leydig cells) of the testis to produce androgens. HCG is composed of an alpha and a beta sub-unit. The alpha sub-unit is essentially identical to the alpha sub units of the human pituitary gonadotropins, luteinizing hormone (LH) and follicle-stimulating hormone (FSH), as well as to the alpha sub-unit of human thyroid-stimulating hormone (TSH), while the beta sub units of these hormones differ in amino acid sequence. As a drug product, chorionic gonadotropin is a highly purified pyrogen-free preparation obtained from the urine of pregnant females.
Indication
For the treatment of prepubertal cryptorchidism (not due to anatomical obstruction), for the treatment of selected cases of hypogonadotropic hypogonadism (hypogonadism secondary to a pituitary deficiency) in males and for the induction of ovulation and pregnancy in the anovulatory, infertile woman in whom the cause of anovulation is secondary and not due to primary ovarian failure, and who has been appropriately pretreated with human menotropins.
Associated Conditions
- Idiopathic Hypogonadotropic Hypogonadism
- Undescended Testis
- Secondary Hypogonadotrophic hypogonadism
Research Report
Comprehensive Report on Chorionic Gonadotropin (Human) (DrugBank ID: DB09126)
I. Introduction to Chorionic Gonadotropin (Human) (DB09126)
A. Overview and Clinical Significance
Chorionic Gonadotropin (Human), commonly referred to as hCG, is a polypeptide hormone naturally synthesized by the syncytiotrophoblast cells of the placenta during pregnancy.[1] As a therapeutic agent, specifically identified by DrugBank ID DB09126, it is formulated as a highly purified, pyrogen-free preparation derived from the urine of pregnant females.[3] The hormone's primary physiological role is the maternal recognition of pregnancy and maintenance of the corpus luteum, ensuring continued progesterone secretion crucial for sustaining the early stages of gestation.[1]
The clinical utility of exogenous hCG stems from its ability to mimic the biological actions of endogenous luteinizing hormone (LH) and, to a lesser extent, follicle-stimulating hormone (FSH).[3] This LH-like activity allows hCG to stimulate gonadal steroid hormone production. Consequently, its principal therapeutic applications include the management of prepubertal cryptorchidism (undescended testes not due to anatomical obstruction) and hypogonadotropic hypogonadism (characterised by deficient pituitary gonadotropin secretion) in selected male populations. In females, hCG is instrumental in inducing final follicular maturation and ovulation in appropriately selected infertile women, often as a critical component of assisted reproductive technology (ART) protocols.[4] The importance of hCG in reproductive medicine is underscored by its direct action on gonadal cells, promoting steroidogenesis and gametogenesis where endogenous gonadotropic support is insufficient or mistimed.
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2025/06/19 | Not Applicable | Not yet recruiting | |||
2025/06/04 | Phase 4 | Recruiting | Fertility Center of Las Vegas | ||
2024/12/31 | Phase 1 | Not yet recruiting | The Fourth Affiliated Hospital of Zhejiang University School of Medicine | ||
2024/12/09 | Phase 3 | Completed | Shakeela Ishrat | ||
2024/11/12 | Phase 4 | Completed | Omayma Ismail Khalaf | ||
2024/08/29 | N/A | Active, not recruiting | |||
2024/07/01 | Not Applicable | Recruiting | Andros Day Surgery Clinic | ||
2024/05/29 | N/A | Not yet recruiting | Centrum Clinic IVF Center | ||
2023/11/24 | Phase 2 | Not yet recruiting | Bedaya Hospital | ||
2023/10/19 | Phase 3 | Completed |
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
---|---|---|---|---|---|
No FDA approvals found for this drug. |
EMA Drug Approvals
Approved Product | Authorization Holder | Status | Issued Date |
---|---|---|---|
No EMA approvals found for this drug. |
HSA Drug Approvals
Approved Product | Manufacturer | Approval Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
No HSA approvals found for this drug. |
NMPA Drug Approvals
Approved Product | Company | Approval Number | Drug Type | Dosage Form | Approval Date |
---|---|---|---|---|---|
No NMPA approvals found for this drug. |
PPB Drug Approvals
Approved Product | Registration No. | Company | Licence No. | Strength | Registration Date |
---|---|---|---|---|---|
No PPB approvals found for this drug. |
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
---|---|---|---|---|---|
No TGA approvals found for this drug. |
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
---|---|---|---|---|---|
CHORIONIC GONADOTROPIN FOR INJECTION, USP | fresenius kabi canada ltd | 02247459 | Powder For Solution - Intramuscular
,
Subcutaneous | 10000 UNIT / VIAL | 9/13/2004 |
PROFASI HP 10000 | emd serono, a division of emd inc., canada | 01925679 | Powder For Solution
,
Kit
,
Liquid - Subcutaneous
,
Intramuscular | 10000 UNIT / VIAL | 12/31/1991 |
PROFASI HP INJ 10000UNIT/VIAL USP | 00598534 | Powder For Solution - Intramuscular | 10000 UNIT / VIAL | 12/31/1984 | |
PREGNYL | organon canada inc. | 02182904 | Powder For Solution
,
Kit - Intramuscular | 10000 UNIT / VIAL | 8/13/1997 |
A.P.L. - PWS-LIQ | wyeth-ayerst canada inc. | 02168936 | Liquid
,
Powder For Solution - Intramuscular | 10000 UNIT / KIT | 11/11/1998 |
APL INJ 1000 IU/ML | ayerst laboratories | 00002291 | Liquid - Intramuscular | 1000 UNIT / ML | 12/31/1951 |
CIMA AEMPS Drug Approvals
Approved Product | Company | Registration Number | Pharmaceutical Form | Prescription Type | Status |
---|---|---|---|---|---|
No CIMA AEMPS (Spain) approvals found for this drug. |
Philippines FDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
No Philippines FDA approvals found for this drug. |
Saudi SFDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
No Saudi SFDA approvals found for this drug. |
Malaysia NPRA Drug Approvals
Approved Product | Company | Registration Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
No Malaysia NPRA approvals found for this drug. |
UK EMC Drug Information
Medicine Name | MA Holder | MA Number | Pharmaceutical Form | Active Ingredient | Authorization Date |
---|---|---|---|---|---|
No UK EMC drug information found for this drug. |
Help Us Improve
Your feedback helps us provide better drug information and insights.