| Symbol | CLSDQ |
|---|---|
| Name | CLEARSIDE BIOMEDICAL, INC. |
| Sector | HEALTH CARE |
| Region | North America |
| Industry | - |
| Address | 30005 United States GA 900 North Point Parkway Suite 200 |
| Telephone | (678) 270-3631 |
| Fax | — |
| — | |
| Website | https://clearsidebio.com/ |
| Incorporation | US |
| Incorporated On | — |
| Employees | — |
| Fiscal Year | 12/31 |
| Public Since | — |
| Exchanges | OTC;NASDAQ |
| Auditor | — |
| Audit Status | AUDITED |
| Reporting Status | Dark: Alternative Reporting Standard |
| CIK | 0001539029 |
| Description | Clearside Biomedical, Inc., a biopharmaceutical company, focuses on the revolutionizing the delivery of therapies to the back of the eye through the suprachoroidal space. The company offers XIPERE, a triamcinolone acetonide injectable suspension for the treatment of macular edema associated with uveitis. It also develops CLS-AX, an axitinib injectable suspension for suprachoroidal injection, which has completed Phase 2 clinical trial to treat wet AMD. The company has a collaboration with bausch + lomb ireland limited, Arctic Vision (Hong Kong) Limited, REGENXBIO, Inc., BioCryst Pharmaceuticals, Inc., and Aura Biosciences, Inc. Additional info from NASDAQ: Additional info from OTC: |
No news found.
| Trial ID | Title | Phase | Indication | Status | Start Date | Completion Date | Source |
|---|---|---|---|---|---|---|---|
| NCT05891548 | Study to Evaluate Suprachoroidally Administered CLS-AX in the Treatment of Neov… | Phase2 | Neovascular Age-related Macular Degeneration | Completed | 2023-05-31 | 2024-08-20 | ClinicalTrials.gov |
| NCT05131646 | Extension Study to Evaluate the Long-term Outcomes of Subjects in the CLS-AX CL… | — | Neovascular Age-related Macular Degeneration | Completed | 2021-10-08 | 2023-01-05 | ClinicalTrials.gov |
| NCT04626128 | Safety and Tolerability Study of Suprachoroidal Injection of CLS-AX Following A… | Phase1 | Neovascular Age-related Macular Degeneration | Completed | 2020-12-15 | 2022-10-13 | ClinicalTrials.gov |
| NCT03203447 | Suprachoroidal Injection of Triamcinolone Acetonide With IVT Anti-VEGF in Subje… | Phase3 | Macular Edema | Terminated | 2018-03-05 | 2018-12-18 | ClinicalTrials.gov |
| NCT02952001 | MAGNOLIA: Extension Study of Patients With Non-infectious Uveitis Who Participa… | — | Uveitis | Completed | 2017-12-13 | 2018-05-22 | ClinicalTrials.gov |
| NCT03126786 | Suprachoroidal CLS-TA With Intravitreal Aflibercept Versus Aflibercept Alone in… | Phase2 | Diabetic Macular Edema | Completed | 2017-07-11 | 2018-04-17 | ClinicalTrials.gov |
| NCT03097315 | Suprachoroidal Injection of CLS-TA in Patients With Non-infectious Uveitis | Phase3 | Uveitis | Completed | 2017-04-04 | 2018-01-24 | ClinicalTrials.gov |
| NCT02980874 | Suprachoroidal Injection of Triamcinolone Acetonide With IVT Aflibercept in Sub… | Phase3 | Macular Edema | Terminated | 2017-01-31 | 2018-12-10 | ClinicalTrials.gov |
| NCT02949024 | Suprachoroidal Injection of CLS-TA Alone or With Aflibercept in Subjects With D… | Phase1 | Diabetic Macular Edema | Completed | 2016-11-10 | 2017-10-17 | ClinicalTrials.gov |
| NCT02956330 | Retrospective Study of the Safety and Efficacy of Patients With RVO in Subjects… | — | Macular Edema | Completed | 2016-11-01 | 2017-04-12 | ClinicalTrials.gov |
| NCT02595398 | Suprachoroidal Injection of CLS-TA in Subjects With Macular Edema Associated Wi… | Phase3 | Uveitis | Completed | 2015-11-17 | 2018-01-18 | ClinicalTrials.gov |
| NCT02303184 | Suprachoroidal Injection of Triamcinolone Acetonide With IVT Aflibercept in Sub… | Phase2 | Macular Edema | Completed | 2015-01-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02255032 | Suprachoroidal Injection of Triamcinolone Acetonide in Subjects With Macular Ed… | Phase2 | Uveitis | Completed | 2014-10-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01789320 | Safety Study of Suprachoroidal Triamcinolone Acetonide Via Microneedle to Treat… | Phase1 | Uveitis | Completed | 2013-02-01 | 2015-03-01 | ClinicalTrials.gov |
| Product Name | Type | Development Stage | Therapeutic Area | Study Status | Trial ID |
|---|---|---|---|---|---|
| triamcinolone acetonide (Triesence®) | Other | Phase PHASE1 | Uveitis | COMPLETED | NCT01789320 |
| Aflibercept | Other | Phase PHASE2 | Neovascular Age-related Macular Degeneration | COMPLETED | NCT05891548 |
| CLS-AX | Other | Phase PHASE2 | Neovascular Age-related Macular Degeneration | COMPLETED | NCT05891548 |
| IVT aflibercept | Other | Phase PHASE2 | Macular Edema | COMPLETED | NCT02303184 |
| Sham | Other | Phase PHASE2 | Macular Edema | COMPLETED | NCT02303184 |
| 4 mg CLS-TA | Other | Phase PHASE2 | Macular Edema | COMPLETED | NCT02303184 |
| 0.8 mg CLS-TA | Other | Phase PHASE2 | Uveitis | COMPLETED | NCT02255032 |
| 4 mg CLS-TA | Other | Phase PHASE2 | Uveitis | COMPLETED | NCT02255032 |
| IVT aflibercept | Other | Phase PHASE3 | Macular Edema | TERMINATED | NCT02980874 |
| suprachoroidal sham | Other | Phase PHASE3 | Macular Edema | TERMINATED | NCT02980874 |
| suprachoroidal CLS-TA | Other | Phase PHASE3 | Macular Edema | TERMINATED | NCT02980874 |
| Lucentis or Avastin | Other | Phase PHASE3 | Macular Edema | TERMINATED | NCT03203447 |
| suprachoroidal sham | Other | Phase PHASE3 | Macular Edema | TERMINATED | NCT03203447 |
| suprachoroidal CLS-TA | Other | Phase PHASE3 | Macular Edema | TERMINATED | NCT03203447 |
| SC CLS-TA | Other | Phase PHASE2 | Diabetic Macular Edema | COMPLETED | NCT03126786 |
| Sham SC | Other | Phase PHASE2 | Diabetic Macular Edema | COMPLETED | NCT03126786 |
| IVT aflibercept | Other | Phase PHASE2 | Diabetic Macular Edema | COMPLETED | NCT03126786 |
| SC CLS-TA | Other | Phase PHASE1 | Diabetic Macular Edema | COMPLETED | NCT02949024 |
| IVT Aflibercept | Other | Phase PHASE1 | Diabetic Macular Edema | COMPLETED | NCT02949024 |
| Sham Procedure | Procedure | Phase PHASE3 | Uveitis | COMPLETED | NCT02595398 |
| 4mg CLS-TA Suprachoriodal Injection | Other | Phase PHASE3 | Uveitis | COMPLETED | NCT02595398 |
| Sham procedure | Procedure | Preclinical | Uveitis | COMPLETED | NCT02952001 |
| 4 mg CLS-TA Suprachoriodal Injection | Other | Preclinical | Uveitis | COMPLETED | NCT02952001 |
| 4 mg CLS-TA Suprachoriodal Injection | Other | Phase PHASE3 | Uveitis | COMPLETED | NCT03097315 |
| Anti-VEGF | Other | Phase PHASE1 | Neovascular Age-related Macular Degeneration | COMPLETED | NCT04626128 |
| CLS-AX | Other | Phase PHASE1 | Neovascular Age-related Macular Degeneration | COMPLETED | NCT04626128 |
| CLS-AX | Other | Preclinical | Neovascular Age-related Macular Degeneration | COMPLETED | NCT05131646 |
| Aflibercept | DRUG | Phase PHASE2 | Neovascular Age-related Macular Degeneration | COMPLETED | NCT05891548 |
| Anti-VEGF | DRUG | Phase PHASE1 | Neovascular Age-related Macular Degeneration | COMPLETED | NCT04626128 |
| CLS-AX | DRUG | Phase PHASE2 | Neovascular Age-related Macular Degeneration | COMPLETED | NCT05891548 |
| Lucentis or Avastin | DRUG | Phase PHASE3 | Macular Edema | TERMINATED | NCT03203447 |
| Sham SC | DRUG | Phase PHASE2 | Diabetic Macular Edema | COMPLETED | NCT03126786 |
| suprachoroidal sham | DRUG | Phase PHASE3 | Macular Edema | TERMINATED | NCT03203447 |
| suprachoroidal CLS-TA | DRUG | Phase PHASE3 | Macular Edema | TERMINATED | NCT03203447 |
| Sham procedure | DRUG | Preclinical | Uveitis | COMPLETED | NCT02952001 |
| 4 mg CLS-TA Suprachoriodal Injection | DRUG | Phase PHASE3 | Uveitis | COMPLETED | NCT03097315 |
| SC CLS-TA | DRUG | Phase PHASE2 | Diabetic Macular Edema | COMPLETED | NCT03126786 |
| IVT Aflibercept | DRUG | Phase PHASE1 | Diabetic Macular Edema | COMPLETED | NCT02949024 |
| Sham Procedure | DRUG | Phase PHASE3 | Uveitis | COMPLETED | NCT02595398 |
| 4mg CLS-TA Suprachoriodal Injection | DRUG | Phase PHASE3 | Uveitis | COMPLETED | NCT02595398 |
| IVT aflibercept | DRUG | Phase PHASE2 | Diabetic Macular Edema | COMPLETED | NCT03126786 |
| Sham | DRUG | Phase PHASE2 | Macular Edema | COMPLETED | NCT02303184 |
| 0.8 mg CLS-TA | DRUG | Phase PHASE2 | Uveitis | COMPLETED | NCT02255032 |
| 4 mg CLS-TA | DRUG | Phase PHASE2 | Macular Edema | COMPLETED | NCT02303184 |
| triamcinolone acetonide (Triesence®) | DRUG | Phase PHASE1 | Uveitis | COMPLETED | NCT01789320 |