Overview
Cetrorelix is a man-made hormone that blocks the effects of Gonadotropin Releasing Hormone (GnRH). GnRH controls another hormone that is called luteinizing hormone (LH), which is the hormone that starts ovulation during the menstrual cycle. When undergoing hormone treatment sometimes premature ovulation can occur, leading to eggs that are not ready for fertilization to be released. Cetrorelix does not allow the premature release of these eggs to occur.
Indication
For the inhibition of premature LH surges in women undergoing controlled ovarian stimulation
Associated Conditions
No associated conditions information available.
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
|---|---|---|---|---|---|
2025/03/11 | Phase 3 | Completed | Kasr El Aini Hospital | ||
2024/09/23 | Phase 1 | Completed | Ahmed Saad | ||
2024/04/22 | Not Applicable | Recruiting | Mỹ Đức Hospital | ||
2023/09/05 | Not Applicable | Recruiting | Northwest Women's and Children's Hospital, Xi'an, Shaanxi | ||
2023/08/02 | Phase 3 | Recruiting | |||
2023/07/19 | Phase 2 | Not yet recruiting | |||
2023/03/02 | Not Applicable | Recruiting | |||
2023/02/22 | Phase 2 | Not yet recruiting | Bio Genuine (Shanghai) Biotech Co., Ltd. | ||
2021/11/09 | Not Applicable | UNKNOWN | |||
2021/08/06 | Phase 4 | UNKNOWN |
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 |
|---|---|---|---|---|---|
| CETROTIDE INJECTION 0.25 mg | SIN11345P | INJECTION | 0.25 mg | 7/10/2000 |
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 |
|---|---|---|---|---|---|
| CETROTIDE cetrorelix 250 microgram (as acetate) powder for injection vial with diluent syringe | 74888 | Medicine | A | 12/19/2000 | |
| Cetrorelix RBX Cetrorelix 250 micrograms/mL Solution for Injection Prefilled Syringe | 444614 | Medicine | A | 3/5/2025 | |
| FEMVI Cetrorelix 250 micrograms/mL Solution for Injection Prefilled Syringe | 444616 | Medicine | A | 3/5/2025 | |
| Cetrorelix SUN Cetrorelix 250 micrograms/mL Solution for Injection Prefilled Syringe | 444615 | Medicine | A | 3/5/2025 |
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
|---|---|---|---|---|---|
| No Health Canada approvals found for this drug. | |||||
CIMA AEMPS Drug Approvals
Approved Product | Company | Registration Number | Pharmaceutical Form | Prescription Type | Status |
|---|---|---|---|---|---|
| CEZIBOE 0,25 MG SOLUCION INYECTABLE EN JERINGA PRECARGADA | 85838 | SOLUCIÓN INYECTABLE EN JERINGA PRECARGADA | Diagnóstico Hospitalario | Commercialized | |
| CETROTIDE 0,25 mg POLVO Y DISOLVENTE PARA SOLUCION INYECTABLE | 99100002 | POLVO Y DISOLVENTE PARA SOLUCIÓN INYECTABLE | Diagnóstico Hospitalario | Not Commercialized | |
| CETROTIDE 0,25 mg POLVO Y DISOLVENTE PARA SOLUCION INYECTABLE | 99100001 | POLVO Y DISOLVENTE PARA SOLUCIÓN INYECTABLE | Diagnóstico Hospitalario | Not Commercialized | |
| CETRORELIX EDEST 0,25 MG POLVO PARA SOLUCION INYECTABLE | Intas Third Party Sales 2005 S.L. | 85740 | POLVO PARA SOLUCIÓN INYECTABLE | Diagnóstico Hospitalario | Not Commercialized |
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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