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Adverum Biotechnologies Reports Fourth Quarter and Full Year 2021 Financial Results

REDWOOD CITY, Calif., March 29, 2022 (GLOBE NEWSWIRE) — Adverum Biotechnologies, Inc. (Nasdaq: ADVM), a clinical-stage gene therapy company targeting unmet medical needs in ocular and rare diseases, today reported financial results for the fourth quarter and full year ended December 31, 2021 and provided a business update. “2022 is on track to be an important year for Adverum, as we progress our plan to initiate a Phase 2 trial evaluating two doses of ADVM-022 in patients with wet age-related macular degeneration,” stated Laurent Fischer, M.D., president and chief executive officer at Adverum Biotechnologies. “Given our robust safety review of all 55 patients treated with ADVM-022, promising clinical efficacy data generated in our OPTIC study in wet age-related macular degeneration and cash runway into 2024, we are able to approach initiating a Phase 2 trial of ADVM-022 with confidence. We are looking forward to dosing the first patient in the third quarter of 2022.” “Additionally, we continue to strengthen our leadership team with multiple senior management hires and board appointments, all of whom are veterans in their respective fields and embrace the vision of Adverum,” Fischer continued, “Together we are committed to advancing ADVM-022’s development and its potential to deliver a one-time, in-office treatment designed to prevent vision loss in wet age-related macular degeneration patients and to offer an alternative to today’s standard of care requiring frequent anti-VEGF injections.” ADVM-022 for Wet Age-Related Macular Degeneration (Wet AMD) Adverum intends to initiate a Phase 2 trial to evaluate two dose levels of ADVM-022, 2 X 10^11 vg/eye (2E11) and a new lower dose 6 X 10^10 vg/eye (6E10), as well as new enhanced prophylactic steroid regimens, which are expected to include local steroids and a combination of local and systemic steroids. Adverum anticipates the study will evaluate endpoints similar to the Phase 1 OPTIC trial in wet AMD. The company expects to dose the first patient in the Phase 2 trial in the third quarter of 2022. Adverum presented two-year follow-up data from its Phase 1 OPTIC trial of ADVM-022 in wet AMD patients at the Retina Society’s 54th Annual Scientific Meeting in October 2021. The data presented demonstrated a greater than 80% reduction in annualized anti-VEGF injections following the 2E11 vg/eye ADVM-022 intravitreal (IVT) injection. Additionally, in patients with wet AMD, ADVM-022 was well-tolerated and ocular inflammation was minimal and responsive to steroid eye drops.   Additional Recent Highlights Adverum was granted Orphan Drug Designation (ODD) by the FDA for ADVM-062 (AAV/7m8-L-opsin), a novel gene therapy product candidate developed as a potential single IVT administration for the treatment of blue cone monochromacy by delivering a functional copy of the OPN1LW gene.Key executive leadership hires include Rupert D’Souza, Ph.D., M.B.A., as chief financial officer, Star Seyedkazemi, Pharm.D., as chief development officer, and Richard Beckman, M.D., as chief medical officer. Jim Wang, Ph.D., M.B.A., who joined the company in August 2021, was recently promoted to chief regulatory officer.Two additions were made to the Board of Directors with the appointments of Rabia Gurses Ozden, M.D. and Soo J. Hong, M.B.A.   Dr. Ozden joins with two decades of experience in ophthalmology, clinical development and operations, pharmacovigilance, regulatory affairs and gene therapy. Ms. Hong brings a deep expertise in human capital management, executive and leadership development as well as executive and board compensation design and governance serving rapidly growing organizations during periods of transformation.     Anticipated 2022 Milestones 2Q 2022 – Presentation of “Phase 1 Study of Intravitreal (IVT) Gene Therapy with ADVM-022 for neovascular AMD (OPTIC Trial): the role of neutralizing antibodies (NAbs)” at The Association for Research in Vision and Ophthalmology (ARVO) Annual Meeting on May 1, 2022, in Denver, CO2Q 2022 – Intend to present non-human primate protein expression data supporting a human equivalent dose of ADVM-022 6 X 10^10 vg/eye (6E10)Mid-2022 – Complete IND amendment process to enable initiation of Phase 2 trial of ADVM-022 in wet AMD3Q 2022 – Plan to dose first patient in an ADVM-022 Phase 2 trial in wet AMD Financial Results for the Three Months Ended December 31, 2021 Cash, cash equivalents and short-term investments were $305.2 million as of December 31, 2021, compared to $332.7 million as of September 30, 2021, and $429.7 million as of December 31, 2020. Adverum expects the year-end cash position to fund operations into 2024.Research and development expenses were $22.5 million for the three months ended December 31, 2021, compared to $22.7 million for the same period in 2020. Research and development expenses were relatively flat primarily due to lower clinical trial costs offset by slightly higher laboratory and consulting expenses. Stock-based compensation expense included in research and development expenses was $1.8 million for the fourth quarter of 2021.General and administrative expenses were $11.9 million for the three months ended December 31, 2021, compared to $13.7 million for the same period in 2020. General and administrative expenses decreased primarily due to lower personnel-associated and professional services costs, partially offset by higher insurance and higher lease expenses for Adverum’s new headquarters. Stock-based compensation expense included in general and administrative expenses was $2.7 million for the fourth quarter of 2021.Net loss was $34.4 million, or $0.35 per basic and diluted share, for the three months ended December 31, 2021, compared to $37.6 million, or $0.39 per basic and diluted share, for the same period in 2020. About Adverum Biotechnologies Adverum Biotechnologies (Nasdaq: ADVM) is a clinical-stage gene therapy company targeting unmet medical needs in serious ocular and rare diseases. Adverum is evaluating its novel gene therapy candidate, ADVM-022, as a one-time, intravitreal injection for the treatment of patients with neovascular or wet age-related macular degeneration. ADVM-062 is a gene therapy candidate specifically designed for patients suffering from blue cone monochromacy. ADVM-062 utilizes Adverum’s propriety vector capsid, AAV.7m8. For more information, please visit www.adverum.com. Forward-looking Statements Statements contained in this press release regarding the events or results that may occur in the future are “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995. Such statements include but are not limited to statements regarding the expected current cash runway into 2024, and the statements under the caption “Anticipated 2022 Milestones” and in the first paragraph under the caption “ADVM-022 for Wet Age-Related Macular Degeneration (Wet AMD).” Actual results could differ materially from those anticipated in such forward-looking statements as a result of various risks and uncertainties, which include risks inherent to, without limitation: Adverum’s novel technology, which makes it difficult to predict the time and cost of product candidate development and obtaining regulatory approval; the results of early clinical trials not always being predictive of future results; and any future complications or side effects in connection with use of ADVM-022, to delay or prevent regulatory advancement or approval for ADVM-022. Additional risks and uncertainties facing Adverum are set forth under the caption “Risk Factors” and elsewhere in Adverum’s Securities and Exchange Commission filings and reports, including Adverum’s Quarterly Report on Form 10-Q for the quarter ended September 30, 2021, and future filings and reports by Adverum, including Adverum’s Annual Report on Form 10-K for the year ended December 31, 2021. All forward-looking statements contained in this press release speak only as of the date on which they were made. Adverum undertakes no obligation to update such statements to reflect events that occur or circumstances that exist after the date on which they were made. Inquiries Anand ReddiVice President, Head of Corporate Strategy and External Affairs & EngagementAdverum Biotechnologies, Inc.T: 650-649-1358 Or Investors:Laurence WattsGilmartin GroupT: 619-916-7620E: laurence@gilmartinir.com Media:Jennifer ArcureCanale CommunicationsT: 917-603-0681E: Jennifer.Arcure@canalecomm.com Source: Adverum Biotechnologies, Inc.  Adverum Biotechnologies, Inc.Consolidated Balance Sheets(In thousands)       December 31December 31   2021   2020   (Unaudited)  (1)Assets    Current assets:    Cash and cash equivalents $34,195  $62,424 Short-term investments  270,993   367,305 Lease incentive receivable  5,709   – Prepaid expenses and other current assets 6,248   4,709 Total current assets  317,145   434,438 Property and equipment, net  33,060   27,725 Operating lease right-of-use asset  86,000   19,376 Restricted cash  2,503   999 Deferred rent receivable  769   – Deposit and other long-term assets  250   29 Total assets $439,727  $482,567      Liabilities and stockholders’ equity    Current liabilities:    Accounts payable $1,387  $2,810 Lease liability, current portion  1,886   4,473 Accrued expenses and other current liabilities  18,047   13,588 Total current liabilities  21,320   20,871 Lease liability, net of current portion  101,108   26,235 Other noncurrent liabilities  1,114   1,114 Total liabilities  123,542   48,220 Stockholders’ equity:    Common stock  10   10 Additional paid-in capital  964,965   937,134 Accumulated other comprehensive loss  (714)  (261)Accumulated deficit  (648,076)  (502,536)Total stockholders’ equity  316,185   434,347 Total liabilities and stockholders’ equity$439,727  $482,567       (1) Derived from Adverum’s annual audited consolidated financial statements.      Adverum Biotechnologies, Inc.Consolidated Statements of Operations(In thousands except per share data)           Three months ended December 31, Years ended December 31,   2021   2020   2021   2020   (Unaudited) (Unaudited)  (1)         License revenue $-  $-  $7,500  $-          Operating expenses:        Research and development  22,524   22,728   89,181   73,309 General and administrative  11,895   13,652   64,441   44,641 Total operating expenses  34,419   36,380   153,622   117,950 Operating loss  (34,419)  (36,380)  (146,122)  (117,950)Other income, net  10   (138)  582   1,557 Net loss before income taxes  (34,409)  (36,518)  (145,540)  (116,393)Income tax provision  –   (1,114)  –   (1,114)Net loss  (34,409)  (37,632)  (145,540)  (117,507)Net loss per share — basic and diluted $(0.35) $(0.39) $(1.48) $(1.38)Weighted-average common shares outstanding – basic and diluted  98,253   97,506   98,039   85,146          (1) Derived from Adverum’s annual audited consolidated financial statements.      

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