Clearside Biomedical Announces Second Quarter 2021 Financial Results and Provides Corporate Update
Clearside Biomedical (NASDAQ:CLSD) announced progress in its clinical trials and financial results for Q2 2021. Key highlights include the initiation of Cohort 2 enrollment in the OASIS Phase 1/2a trial for wet AMD, achieving safety endpoints in Cohort 1. The FDA set a PDUFA date of October 30, 2021, for XIPERE's NDA review, aiming to treat macular edema associated with uveitis. For Q2 2021, Clearside reported revenues of $0.8 million, up from $0.4 million in Q2 2020, alongside a net loss of $6.1 million, or $0.11 per share, compared to $5.8 million, or $0.13 per share, in the previous year.
- Successfully advanced to Cohort 2 in the OASIS trial for wet AMD with an increased dosage.
- Achieved safety and tolerability in Cohort 1 of the OASIS trial.
- FDA accepted the NDA resubmission for XIPERE, with a PDUFA action date set for October 30, 2021.
- Increased revenue from licensing agreements, reporting $0.8 million in Q2 2021.
- Net loss widened to $6.1 million in Q2 2021 compared to $5.8 million in Q2 2020.
- Research and development expenses rose to $4.1 million, reflecting higher costs without immediate revenue generation.
- Enrollment Underway in Cohort 2 of OASIS Wet AMD Phase 1/2a Trial with Data Expected by the End of 2021 –
- Upcoming FDA PDUFA Action Date in October 2021 for XIPERE™ (triamcinolone acetonide suprachoroidal injectable suspension) -
- Management to Host Webcast and Conference Call Today at 4:30 P.M. ET -
ALPHARETTA, Ga., Aug. 10, 2021 (GLOBE NEWSWIRE) -- Clearside Biomedical, Inc. (NASDAQ:CLSD), a biopharmaceutical company dedicated to developing and delivering treatments that restore and preserve vision for people with serious back of the eye diseases, today reported financial results for second quarter ended June 30, 2021.
“We continue to demonstrate our position as the leader in the suprachoroidal space with numerous clinical trials in multiple indications, a New Drug Application (NDA) for XIPERE™ under regulatory review and recent positive results from our CLS-AX clinical trial,” said George Lasezkay, Pharm.D., J.D., Clearside’s President and Chief Executive Officer. “We are the first company to develop a clinically tested, non-surgical, repeatable micro-injection technology designed to unlock the potential clinical benefits of administering drugs into the suprachoroidal space. We are encouraged by the Cohort 1 results of our OASIS Phase 1/2a trial in wet AMD patients, which achieved its safety and tolerability endpoints. We believe the Cohort 1 data supports our hypothesis that the combination of targeted and compartmentalized suprachoroidal delivery and the potent pan-VEGF attributes of axitinib may facilitate an effective treatment option for patients suffering from wet AMD. We have begun enrollment in Cohort 2 with more than triple the dose used in Cohort 1 and look forward to reporting results by the end of 2021.”
“Following our NDA resubmission for XIPERE for the treatment of macular edema associated with uveitis, the U.S. Food and Drug Administration (FDA) assigned a Prescription Drug User Fee Act (PDUFA) action date of October 30, 2021. If approved, XIPERE would represent the first therapy for macular edema associated with uveitis, the first approved therapeutic delivered into the suprachoroidal space and the first commercial product developed by Clearside. In addition to progressing our internal development initiatives, we continue to work closely with our commercial and drug development partners, and expect data from their ongoing clinical trials using our SCS Microinjector® later this year,” concluded Dr. Lasezkay.
Key Highlights
- Patient enrollment is underway in Cohort 2 of OASIS, Clearside’s U.S. based, open-label, dose-escalation Phase 1/2a trial in wet AMD patients, to assess the safety and tolerability of a 0.1 mg dose of CLS-AX administered by suprachoroidal injection via Clearside’s SCS Microinjector®.
- Clearside reported positive results from Cohort 1 of OASIS in six patients (n=6) with neovascular age-related macular degeneration (wet AMD). The primary endpoints were achieved in Cohort 1, as the initial lowest planned dose of 0.03 mg CLS-AX was well tolerated with no serious adverse events and no drug related treatment emergent adverse events observed throughout the study period.
- FDA accepted the XIPERE NDA resubmission and assigned a PDUFA action date of October 30, 2021.
- Multiple presentations featuring the use of Clearside’s proprietary suprachoroidal space (SCS®) delivery platform to administer small molecules and gene therapy were highlighted at global conferences, including the Association for Research in Vision and Ophthalmology (ARVO) Annual Meeting and the Wet AMD & DME Drug Development Summit.
- Data was published in Translational Vision Science & Technology titled “Evaluation of Long-Lasting Potential of Suprachoroidal Axitinib Suspension Via Ocular and Systemic Disposition in Rabbits” in June 2021.
Second Quarter 2021 Financial Results
Clearside’s license and other revenue for the second quarter of 2021 was
Research and development expenses for the second quarter of 2021 were
General and administrative expenses for the second quarter of 2021 were
Net loss for the second quarter of 2021 was
As of June 30, 2021, Clearside’s cash and cash equivalents totaled
Conference Call & Webcast Details
Clearside’s management will host a webcast and conference call today at 4:30 p.m. Eastern Time to discuss the financial results and provide a corporate update. The live and archived webcast may be accessed on the Clearside website under the Investors section: Events and Presentations. The live call can be accessed by dialing (844) 263-8310 (domestic) or (213) 358-0959 (international) and entering conference code: 7785213. An archive of the webcast will be available for three months.
About Clearside Biomedical
Clearside Biomedical, Inc. is a biopharmaceutical company dedicated to developing and delivering treatments that restore and preserve vision for people with serious back of the eye diseases. Clearside’s proprietary SCS Microinjector® targets the suprachoroidal space (SCS®) and offers unique access to the macula, retina and choroid where sight-threatening disease often occurs. The Company’s SCS injection platform is an inherently flexible, in-office, non-surgical procedure, intended to provide targeted delivery to the site of disease and to work with both established and new formulations of medications. For more information, please visit www.clearsidebio.com.
Cautionary Note Regarding Forward-Looking Statements
Any statements contained in this press release that do not describe historical facts may constitute forward-looking statements as that term is defined in the Private Securities Litigation Reform Act of 1995. These statements may be identified by words such as “believe”, “expect”, “may”, “plan”, “potential”, “will”, and similar expressions, and are based on Clearside’s current beliefs and expectations. These forward-looking statements include statements regarding the clinical development, including the timing of data from the OASIS clinical trial, the potential benefits of XIPERE, CLS-AX and therapies using Clearside’s SCS Microinjector®, the resubmitted NDA for and anticipated regulatory approval of XIPERE and Clearside’s ability to fund its operations into the second quarter of 2022. These statements involve risks and uncertainties that could cause actual results to differ materially from those reflected in such statements. Risks and uncertainties that may cause actual results to differ materially include uncertainties inherent in the conduct of clinical trials, Clearside’s reliance on third parties over which it may not always have full control, uncertainties regarding the COVID-19 pandemic and other risks and uncertainties that are described in Clearside’s Annual Report on Form 10-K for the year ended December 31, 2020, filed with the U.S. Securities and Exchange Commission (“SEC”) on March 15, 2021, and Clearside’s other Periodic Reports filed with the SEC. Any forward-looking statements speak only as of the date of this press release and are based on information available to Clearside as of the date of this release, and Clearside assumes no obligation to, and does not intend to, update any forward-looking statements, whether as a result of new information, future events or otherwise.
Investor and Media Contacts:
Jenny Kobin
Remy Bernarda
ir@clearsidebio.com
(678) 430-8206
-Financial Tables Follow-
| CLEARSIDE BIOMEDICAL, INC. | ||||||||||||||||
| Selected Financial Data | ||||||||||||||||
| (in thousands, except share and per share data) | ||||||||||||||||
| (unaudited) | ||||||||||||||||
| Statements of Operations Data | Three Months Ended June 30, | Six Months Ended June 30, | ||||||||||||||
| 2021 | 2020 | 2021 | 2020 | |||||||||||||
| License and other revenue | $ | 780 | $ | 354 | $ | 814 | $ | 4,451 | ||||||||
| Operating expenses: | ||||||||||||||||
| Research and development | 4,060 | 3,300 | 9,550 | 7,111 | ||||||||||||
| General and administrative | 2,816 | 2,611 | 5,709 | 5,733 | ||||||||||||
| Total operating expenses | 6,876 | 5,911 | 15,259 | 12,844 | ||||||||||||
| Loss from operations | (6,096 | ) | (5,557 | ) | (14,445 | ) | (8,393 | ) | ||||||||
| Other income | 1 | — | 999 | — | ||||||||||||
| Other expense | — | (197 | ) | — | (272 | ) | ||||||||||
| Net loss | $ | (6,095 | ) | $ | (5,754 | ) | $ | (13,446 | ) | $ | (8,665 | ) | ||||
| Net loss per share of common stock — basic and diluted | $ | (0.11 | ) | $ | (0.13 | ) | $ | (0.23 | ) | $ | (0.19 | ) | ||||
| Weighted average shares outstanding — basic and diluted | 57,745,465 | 45,214,500 | 57,394,017 | 44,984,005 | ||||||||||||
| Balance Sheet Data | June 30, | December 31, | |||
| 2021 | 2020 | ||||
| Cash and cash equivalents | $ | 26,414 | $ | 17,287 | |
| Total assets | 28,592 | 19,322 | |||
| Deferred revenue | 5,000 | 5,000 | |||
| Long-term debt (including current portion) | — | 991 | |||
| Total liabilities | 9,254 | 10,559 | |||
| Total stockholders’ equity | 19,338 | 8,763 | |||
Source: Clearside Biomedical, Inc.
FAQ
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