Last reviewed · How we verify
Cialis (tadalafil)
At a glance
| Generic name | tadalafil |
|---|---|
| Sponsor | Eli Lilly |
| Drug class | Phosphodiesterase 5 Inhibitor [EPC] |
| Target | Nuclear receptor subfamily 2 group E member 1, Dual 3',5'-cyclic-AMP and -GMP phosphodiesterase 11A, Potassium voltage-gated channel subfamily H member 2 |
| Therapeutic area | Urology |
| Phase | FDA-approved |
Approved indications
- Benign prostatic hyperplasia
- Impotence
- Pulmonary hypertension
Common side effects
- Headache
- Dyspepsia
- Back pain
- Myalgia
- Nasal congestion
- Flushing
- Pain in limb
Serious adverse events
- Gastroesophageal reflux disease
- Vomiting
- Arthralgia
- Muscle spasm
Key clinical trials
- Randomised Control Trial to Assess the Efficacy of Tadalafil in Raynaud's Phenomenon in Scleroderma (Phase 3)
- Medication Facilitated Ureteral Access Sheath Deployment During Ureteroscopy and Endoscopic-Guided Percutaneous Nephrolithotomy: A Randomized Double-Blind Placebo Controlled Trial of Tadalafil, Tamsul (Phase 4)
- NCT03246880 (Phase 3)
- Pilot Study to Investigate the Effect of Tadalafil on Secondary Pulmonary Hypertension in Chronic Obstructive Pulmonary Disease (NA)
- Phase I Trial of Chemoimmunotherapy and Hypofractionated Radiation Therapy for Borderline Resectable and Locally Advanced Pancreatic Adenocarcinoma. (Phase 1)
- Do Phosphodiesterase 5A Inhibitors Improve Exercise Capacity in Patients With Chronic Obstructive Pulmonary Disease and Pulmonary Hypertension? (Phase 2)
- Efficacy of Tadalafil and Solifenacin Versus Tamsulosin and Solifenacin Combination Therapy for the Treatment of Benign Prostatic Hyperplasia With Overactive Bladder: A Randomized Controlled Trial (Phase 4)
- A Randomized, Open-label, Multiple Dosing, 2-way Crossover Study to Evaluate the Pharmacokinetic Effect of Tadalafil on Tamsulosin in Healthy Male Volunteers (Phase 1)
Patents
| Patent | Expiry | Type |
|---|---|---|
| 11975006 | 2038-12-24 | Formulation |
| 12186322 | 2038-12-24 | Formulation |
| 11382917 | 2038-12-24 | Formulation |
| 11666576 | 2038-12-24 | Formulation |
Primary sources
Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.
| Source | Used for |
|---|---|
| ClinicalTrials.gov | Trial enrolment, design, endpoints, results |
| FDA Orange Book | Patents + exclusivity |