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Chorionic Gonadotropin (Human)

Generic Name
Chorionic Gonadotropin (Human)
Brand Names
Novarel, Pregnyl
Drug Type
Biotech
CAS Number
9002-61-3
Unique Ingredient Identifier
20ED16GHEB

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

Published: Jun 4, 2025

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.

Continue reading the full research report

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.

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