Overview
Vardenafil is a selective inhibitor of cyclic guanosine monophosphate (cGMP)-specific phosphodiesterase type 5 (PDE5) and an oral therapy for the treatment of erectile dysfunction. During sexual stimulation, nitric oxide (NO) is released from nerve endings and endothelial cells in the corpus cavernosum, activating the enzyme guanylate cyclase and increasing the synthesis of cGMP in the smooth muscle cells of the corpus cavernosum. PDE5 inhibitors, such as vardenafil, inhibit the degradation of cGMP and allow increased blood flow into the penis, resulting in an erection.. Compared to sildenafil and tadalafil, vardenafil is a more potent inhibitor of PDE5; however, its selectivity for other PDE isoforms is lower than the one detected for tadalafil. The FDA approved the use of vardenafil for the treatment of erectile dysfunction in 2003. Although other PDE5 inhibitors such as sildenafil and tadalafil have been associated with rare cases of acute liver injury, the use of vardenafil has not been linked to hepatotoxic effects. The use of vardenafil as a monotherapy for the treatment of pulmonary arterial hypertension has also been evaluated.
Indication
Vardenafil is indicated for the treatment of erectile dysfunction.
Associated Conditions
- Erectile Dysfunction
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2025/03/06 | Phase 1 | Completed | |||
2024/07/08 | Phase 3 | Recruiting | |||
2022/10/05 | Phase 1 | Completed | |||
2017/04/05 | Phase 1 | UNKNOWN | |||
2015/05/21 | Phase 4 | Completed | |||
2015/01/26 | Phase 4 | UNKNOWN | |||
2014/10/31 | Early Phase 1 | Terminated | |||
2014/08/19 | Phase 2 | Completed | Azienda USL Modena | ||
2012/07/25 | Phase 4 | UNKNOWN | |||
2011/08/01 | N/A | TEMPORARILY_NOT_AVAILABLE |
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
---|---|---|---|---|---|
QYK BRANDS LLC | 73750-104 | ORAL | 10 mg in 1 1 | 3/31/2022 | |
Macleods Pharmaceuticals Limited | 33342-203 | ORAL | 11.85 mg in 1 1 | 9/30/2023 | |
Zydus Pharmaceuticals USA Inc. | 70710-1068 | ORAL | 2.5 mg in 1 1 | 5/30/2023 | |
Zydus Lifesciences Limited | 70771-1048 | ORAL | 5 mg in 1 1 | 10/31/2022 | |
Macleods Pharmaceuticals Limited | 33342-154 | ORAL | 20 mg in 1 1 | 4/10/2023 | |
Macleods Pharmaceuticals Limited | 33342-151 | ORAL | 2.5 mg in 1 1 | 4/10/2023 | |
Macleods Pharmaceuticals Limited | 33342-153 | ORAL | 10 mg in 1 1 | 4/10/2023 | |
QYK BRANDS LLC | 73750-102 | ORAL | 2.5 mg in 1 1 | 3/31/2022 | |
QYK BRANDS LLC | 73750-103 | ORAL | 5 mg in 1 1 | 3/31/2022 | |
Alembic Pharmaceuticals Inc. | 62332-235 | ORAL | 10 mg in 1 1 | 9/15/2023 |
EMA Drug Approvals
Approved Product | Authorization Holder | Status | Issued Date |
---|---|---|---|
Authorised | 3/6/2003 |
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 |
---|---|---|---|---|---|
Vardenafil Hydrochloride Tablets | 国药准字H20249431 | 化学药品 | 片剂 | 11/22/2024 | |
Vardenafil Hydrochloride Tablets | 国药准字H20233690 | 化学药品 | 片剂 | 6/7/2023 | |
Vardenafil Hydrochloride Tablets | 国药准字H20249572 | 化学药品 | 片剂 | 12/1/2024 | |
Vardenafil Hydrochloride Tablets | 国药准字H20233768 | 化学药品 | 片剂 | 6/21/2023 | |
Vardenafil Hydrochloride Tablets | 国药准字H20243124 | 化学药品 | 片剂 | 1/30/2024 | |
Vardenafil Hydrochloride Tablets | 国药准字H20203338 | 化学药品 | 片剂 | 7/21/2020 | |
Vardenafil Hydrochloride Tablets | 国药准字H20203339 | 化学药品 | 片剂 | 7/21/2020 | |
Vardenafil Hydrochloride Tablets | 国药准字H20249029 | 化学药品 | 片剂 | 10/9/2024 | |
Vardenafil Hydrochloride Tablets | 国药准字H20244792 | 化学药品 | 片剂 | 9/3/2024 | |
Vardenafil Hydrochloride Tablets | 国药准字H20243123 | 化学药品 | 片剂 | 1/30/2024 |
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 |
---|---|---|---|---|---|
VARDENAFIL APOTEX vardenafil (as hydrochloride trihydrate) 10 mg film coated tablet blister pack | 289159 | Medicine | A | 3/26/2018 | |
APO-VARDENAFIL vardenafil (as hydrochloride trihydrate) 20 mg film coated tablet blister pack | 289163 | Medicine | A | 3/26/2018 | |
APO-VARDENAFIL vardenafil (as hydrochloride trihydrate) 10 mg film coated tablet blister pack | 289161 | Medicine | A | 3/26/2018 | |
APO-VARDENAFIL vardenafil (as hydrochloride trihydrate) 5 mg film coated tablet blister pack | 289160 | Medicine | A | 3/26/2018 | |
VARDENAFIL APOTEX vardenafil (as hydrochloride trihydrate) 20 mg film coated tablet blister pack | 289162 | Medicine | A | 3/26/2018 | |
VARDENAFIL APOTEX vardenafil (as hydrochloride trihydrate) 5 mg film coated tablet blister pack | 289164 | Medicine | A | 3/26/2018 |
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