Graybug Vision Reports Full Year 2021 Financial Results and Recent Corporate Developments
Graybug Vision, Inc. (NASDAQ: GRAY) reported a net loss of $35.8 million for 2021, up from $27.5 million in 2020. R&D expenses decreased to $18.9 million from $21.0 million, while general and administrative expenses rose notably to $17.0 million. Key advancements include the completion of the ALTISSIMO Phase 2b trial for GB-102, demonstrating a six-month treatment duration in 48% of patients. The company is preparing for a new Phase 2 trial and aims to initiate the GB-401 Phase 1 trial in 2023. The upcoming R&D Day is scheduled for March 30, 2022.
- Completion of ALTISSIMO Phase 2b trial with 48% of patients showing six-month duration with GB-102.
- New enhanced formulation of GB-102 aims to improve safety and efficacy in future trials.
- Anticipated milestones include Phase 2 trial readiness in second half of 2022 for GB-102.
- Net loss increased to $35.8 million from $27.5 million year-over-year.
- General and administrative expenses surged to $17.0 million, partly due to increased stock-based compensation.
Management to host R&D Day for investors on March 30, 2022 at 11 a.m. ET
BALTIMORE, March 10, 2022 (GLOBE NEWSWIRE) -- Graybug Vision, Inc. (Nasdaq: GRAY), a clinical-stage biopharmaceutical company focused on developing transformative medicines for the treatment of ocular diseases, today provided an update on recent corporate developments and reported financial results for the full year ended December 31, 2021.
“Graybug made important progress in advancing its retina (GB-102) and glaucoma (GB-401) programs in 2021. We developed a new enhanced formulation of GB-102 that capitalizes on the duration demonstrated by our Phase 2b ALTISSIMO trial, where half of patients were controlled for six months after a single intravitreal (IVT) injection,” said Frederic Guerard, PharmD, Chief Executive Officer of Graybug Vision. “We are in ongoing discussions to partner GB-102 for its next clinical trial, while finalizing the preparation of an IND application for our GB-401 implant formulation, and pursuing other novel ocular therapeutics.”
Recent Corporate Developments
- Completed ALTISSIMO Phase 2b trial in wet age-related macular degeneration (wet AMD) — Final results confirm unprecedented duration in an aflibercept-controlled clinical trial. GB-102 1mg demonstrated six-month duration in
48% of patients and 12 months in30% of patients, with well-controlled central subretinal thickness (CST), as compared to aflibercept. Best corrected visual acuity (BCVA) of patients in the GB-102 1mg arm trended lower than aflibercept’s, mainly driven by 4 subjects. These subjects had a combination of high anti-VEGF need prior to enrollment, particle dispersion during the study, or adverse events unrelated to the drug, which we expect to address in the next trial with optimized inclusion and rescue criteria, and our new enhanced formulation. - Ongoing partnering discussions to support funding of additional GB-102 wet-AMD clinical trials — New enhanced formulation of GB-102 to further reduce or eliminate microparticle dispersion has been developed, and design of future Phase 2 trial to evaluate safety, efficacy, and durability has been finalized.
- Developed lead GB-401 formulation and custom pre-loaded applicator — Expanded biodegradable polymer platform technology with implant formulation of GB-401, which has the potential to be administered IVT once every six months with a pre-loaded applicator to reduce elevated intraocular pressure in glaucoma patients, is currently in a repeat-dose GLP-tox study.
- Pursuing expansion of pipeline with focus on early-stage novel therapeutics addressing unmet ophthalmic needs — In-licensing efforts targeted at capital-efficient development opportunities are expected to both leverage and expand current platform technologies.
Anticipated Milestones
- Enhanced GB-102 formulation ready for Phase 2 trial in patients with wet AMD as soon as second half of 2022.
- Initiate GB-401, a proprietary implant formulation of a beta-adrenergic receptor inhibitor designed for IVT injection once every six months, Phase 1 trial in first half 2023.
Full Year 2021 Financial Results
Net loss for 2021 was
Research and development expense for 2021 was
General and administrative expense for 2021 was
As of December 31, 2021, the company’s cash, cash equivalents, and short-term investments totaled
R&D Day for Investors
Management plans to host an Investor R&D Day on March 30, 2022 from 11 a.m. to 12:45 p.m. ET. The meeting will feature updates on the company’s advancing pipeline of transformative medicines for the treatment of ocular diseases. Speakers will include Graybug management and key opinion leaders in ophthalmology. A link to attendee registration and additional details about the meeting will be coming soon and will be made available in the Investors and Media section of the company’s website at https://investors.graybug.vision/news-events/events-presentations.
About Graybug
Graybug is a clinical-stage biopharmaceutical company focused on developing transformative medicines for the treatment of ocular diseases. The company’s proprietary ocular delivery technologies are designed to maintain effective drug levels in ocular tissue for six months and potentially longer, improving disease management, reducing healthcare burdens and ultimately delivering better clinical outcomes. Graybug’s lead product candidate, GB-102, a formulation of the pan-vascular endothelial growth factor (VEGF) inhibitor, sunitinib malate targeting a six-month or longer dosing regimen, inhibits multiple neovascular pathways for the intravitreal treatment of retinal diseases, including wet age-related macular degeneration. Graybug’s other product candidates developed using its proprietary technologies also include GB-401, a proprietary implant formulation of a beta-adrenergic blocker prodrug, for primary open-angle glaucoma, with a dosing regimen of once every six months. Founded in 2011 on the basis of technology licensed from the Johns Hopkins University School of Medicine, with offices in Baltimore, Maryland, and Redwood City, California. For more information, please visit www.graybug.vision.
Forward-Looking Statements
This press release contains forward-looking statements within the meaning of the “safe harbor” provisions of the Private Securities Litigation Reform Act of 1995 including, but not limited to, statements regarding the company’s clinical pipeline, its ability to timely identify a partner to fund further development of GB-102 for wet AMD on reasonable terms if at all, its ability to successfully execute one or more other licensing arrangements, the timing or outcomes of its interactions with regulatory authorities, its ability to advance GB-102, GB-401, or any future product candidate through preclinical or clinical development, its ability to achieve its anticipated milestones within the timing outlined above or at all, its ability to conduct planned operations within the evolving constraints arising from the COVID-19 pandemic, the company’s operating results and use of cash, the company’s operations as a public company, the company’s management and board of directors, and the timing, cost, and results of its clinical trials. Forward-looking statements are subject to risks and uncertainties that may cause the company’s actual activities or results to differ significantly from those expressed in any forward-looking statement, including risks and uncertainties described under the heading “Risk Factors” in the company’s quarterly report on Form 10-Q for the three months ended September 30, its annual report on Form 10-K to be filed for the year ended December 31, 2021, and other reports the company files from time to time with the Securities and Exchange Commission. These forward-looking statements speak only as of the date of this press release, and the company undertakes no obligation to revise or update any forward-looking statements to reflect events or circumstances after the date hereof.
| Investor Contact IR@graybug.vision (650) 487-2409 | Media Contact media@graybug.vision (404) 384-0067 |
GRAYBUG VISION, INC.
Condensed Statements of Operations
(In thousands, except share and per share amounts)
(2021 unaudited)
| Year Ended December 31, | ||||||||
| 2021 | 2020 | |||||||
| Operating expenses: | ||||||||
| Research and development | $ | 18,903 | $ | 20,962 | ||||
| General and administrative | 17,044 | 8,870 | ||||||
| Total operating expenses | 35,947 | 29,832 | ||||||
| Loss from operations | (35,947 | ) | (29,832 | ) | ||||
| Interest income | 126 | 143 | ||||||
| Change in fair value of preferred stock tranche obligation | — | 2,158 | ||||||
| Net loss | (35,821 | ) | (27,531 | ) | ||||
| Cumulative dividends on convertible preferred stock | — | (7,189 | ) | |||||
| Net loss attributable to common stockholders | $ | (35,821 | ) | $ | (34,720 | ) | ||
| Net loss per common share—basic and diluted | $ | (1.69 | ) | $ | (5.25 | ) | ||
| Weighted-average number of shares outstanding used in computing net loss per common share—basic and diluted | 21,199,291 | 6,618,445 | ||||||
GRAYBUG VISION, INC.
Condensed Balance Sheets
(In thousands)
(2021 unaudited)
| December 31, | ||||||||
| 2021 | 2020 | |||||||
| Assets | ||||||||
| Current assets: | ||||||||
| Cash and cash equivalents | $ | 13,364 | $ | 33,418 | ||||
| Short-term investments | 50,306 | 61,615 | ||||||
| Prepaid expenses and other current assets | 3,408 | 4,207 | ||||||
| Total current assets | 67,078 | 99,240 | ||||||
| Property and equipment, net | 1,981 | 1,946 | ||||||
| Prepaid expenses and other non-current assets | 29 | 608 | ||||||
| Total assets | $ | 69,088 | $ | 101,794 | ||||
| Liabilities and Stockholders’ Equity | ||||||||
| Current liabilities: | ||||||||
| Accounts payable | $ | 527 | $ | 2,513 | ||||
| Accrued research and development | 304 | 1,356 | ||||||
| Other current liabilities | 3,226 | 3,128 | ||||||
| Total current liabilities | 4,057 | 6,997 | ||||||
| Deferred rent, long term portion | 8 | 11 | ||||||
| Total liabilities | 4,065 | 7,008 | ||||||
| Commitments and contingencies | ||||||||
| Stockholders’ Equity: | ||||||||
| Common stock | 2 | 2 | ||||||
| Additional paid-in capital | 234,225 | 228,155 | ||||||
| Accumulated deficit | (169,188 | ) | (133,367 | ) | ||||
| Accumulated other comprehensive loss | (16 | ) | (4 | ) | ||||
| Total stockholders’ equity | 65,023 | 94,786 | ||||||
| Total liabilities and stockholders’ equity | $ | 69,088 | $ | 101,794 | ||||
FAQ
What were Graybug Vision's financial results for 2021?
What is the status of GB-102 after the ALTISSIMO trial?
When is the next planned trial for GB-401?
When will the R&D Day for investors take place?
