Full Press Release Details
Taysha Gene Therapies Reports Second Quarter 2022 Financial Results and Provides Corporate Update
TSHA-120 treated patients in GAN demonstrated durable improvement and recoverability of
sensory nerve amplitude potential (SNAP), a definitive clinical endpoint, compared to natural history
TSHA-120 commercial grade and clinical trial material considered comparable across all key quality attributes as assessed by an extensive panel of release assays and next-generation sequencing
Positive feedback from MHRA supports regulatory strategy and manufacturing approach including potency assay matrix; additional regulatory
feedback, including from FDA, expected by year-end 2022
Preclinical data for TSHA-102 in Rett syndrome demonstrated near normalization of survival as well as normalization of behavior in neonatal knockout Rett mice; clinical data expected by year-end
Conference call and live webcast today at 8:00 AM Eastern Time
Dallas August 11, 2022 - Taysha Gene Therapies, Inc. (Nasdaq: TSHA), a patient-centric, pivotal-stage gene therapy company
focused on developing and commercializing AAV-based gene therapies for the treatment of monogenic diseases of the central nervous system (CNS) in both rare and large patient populations, today reported
financial results for the second quarter ended June 30, 2022, and provided a corporate update.
We are excited to announce important progress
in giant axonal neuropathy (GAN) including stabilization and improvement of sensory nerve function, a definitive clinical endpoint, in patients with GAN following treatment with TSHA-120, said RA Session
II, President, Founder and CEO of Taysha. In addition, we now have positive comparability data demonstrating that our commercial grade and clinical trial material are comparable across all key quality attributes. Importantly, we believe
positive feedback received from the MHRA, in conjunction with robust comparability data for TSHA-120 and comprehensive clinical data generated to date, further support our ongoing regulatory engagement. We
expect additional regulatory feedback, including from the FDA, by year-end. In Rett syndrome, we are highly encouraged by late-breaking neonatal data in preclinical mouse models demonstrating near
normalization of survival and normalization of behavior. We look forward to reporting preliminary Phase 1/2 clinical data in adult females with Rett syndrome by year-end 2022.
Recent Corporate Highlights
TSHA-120 for giant axonal neuropathy (GAN): an intrathecally dosed AAV9 gene therapy in clinical development for the rare inherited genetic disorder GAN. TSHA-120
has received orphan drug and rare pediatric disease designations from the FDA and orphan drug designation from the European Commission.
syndrome: a self-complementary intrathecally delivered AAV9 gene replacement therapy in clinical development for Rett syndrome. TSHA-102 utilizes the novel miRNA-Responsive
Auto-Regulatory Element (miRARE) platform to regulate transgene expression genotypically on a cell-by-cell basis. TSHA-102 is the
first-and-only gene therapy in clinical development for Rett syndrome. TSHA-102 has received orphan drug and rare pediatric
disease designations from the FDA and has been granted orphan drug designation from the European Commission.
Anticipated 2022 Milestones
Second Quarter 2022 Financial Highlights
Development (R&D) Expenses: Research and development expenses were $23.1 million for the three months ended June 30, 2022, compared to $30.6 million for the three months ended June 30, 2021. The $7.5 million decrease
was primarily attributable to a decrease of $3.8 million in third-party R&D, primarily related to GLP toxicology studies, a decrease of $3.2 million in R&D manufacturing costs, and lower employee compensation expenses of
General and Administrative (G&A) Expenses: General and administrative expenses were
$9.9 million for the three months ended June 30, 2022, compared to $10.1 million for the three months ended June 30, 2021. The decrease of approximately $0.2 million was primarily attributable to a decrease of
$1.1 million in professional fees related to market research, recruiting, accounting, and patient advocacy activities. This was partially offset by $0.9 million of incremental employee compensation expenses.
Net loss: Net loss for the three months ended June 30, 2022, was $33.9 million, or $0.84 per share, as compared to a
net loss of $40.9 million, or $1.09 per share, for the three months ended June 30, 2021.
equivalents: As of June 30, 2022, the Company had cash and cash equivalents of $66.2 million. Taysha continues to expect that its current cash and cash equivalents, in addition to full access to its existing term loan facility, is
sufficient to fund operating expenses into the fourth quarter of 2023.
Conference Call and Webcast Information
Taysha management will hold a conference call and webcast with slides today at 8:00 am ET / 7:00 am CT to review its financial and
operating results and to provide a corporate update. The dial-in number for the conference call is 877-407-0792 (U.S./Canada) or 201-689-8263 (international). The conference ID for all callers is 13730848. The live webcast and replay may be accessed by visiting Taysha s website
at https://ir.tayshagtx.com/news-events/events-presentations. An archived version of the webcast will be available on the website for 30 days.
About Taysha Gene Therapies
Taysha Gene Therapies
(Nasdaq: TSHA) is on a mission to eradicate monogenic CNS disease. With a singular focus on developing curative medicines, we aim to rapidly translate our treatments from bench to bedside. We have combined our team s proven experience in gene
therapy drug development and commercialization with the world-class UT Southwestern Gene Therapy Program to build an extensive, AAV gene therapy pipeline focused on both rare and large-market indications. Together, we leverage our fully integrated
platform an engine for potential new cures with a goal of dramatically improving patients lives. More information is available at www.tayshagtx.com.
Forward-Looking Statements
This press release contains
forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Words such as anticipates, believes, expects, intends, projects, plans,
and future or similar expressions are intended to identify forward-looking statements. Forward-looking statements include statements concerning the potential of our product candidates, including our preclinical product candidates, to
positively impact quality of life and alter the course of disease in the patients we seek to treat, our research, development and regulatory plans for our product candidates, the potential for these product candidates to receive regulatory approval
from the FDA or equivalent foreign regulatory agencies, and whether, if approved, these product candidates will be successfully distributed and marketed, the potential market opportunity for these product candidates, our corporate growth plans, the
forecast of our cash runway and the implementation and potential impacts of our strategic pipeline prioritization initiatives. Forward-looking statements are based on
management s current expectations and are subject to various risks and uncertainties that could cause actual results to differ materially and adversely from those expressed or implied by
such forward-looking statements. Accordingly, these forward-looking statements do not constitute guarantees of future performance, and you are cautioned not to place undue reliance on these forward-looking statements. Risks regarding our business
are described in detail in our Securities and Exchange Commission ( SEC ) filings, including in our Annual Report on Form 10-K for the full-year ended December 31, 2021, and our Quarterly Report
on Form 10-Q for the quarter ended June 30, 2022, both of which are available on the SEC s website at www.sec.gov. Additional information will be made available in other filings that we
make from time to time with the SEC. Such risks may be amplified by the impacts of the COVID-19 pandemic. These forward-looking statements speak only as of the date hereof, and we disclaim any obligation to
update these statements except as may be required by law.
Taysha Gene Therapies, Inc.
Condensed Consolidated Statements of Operations
(in thousands, except share and per share data)
| For the Three Months Ended June 30, | For the Six Months Ended June 30, | |||||||||||||||
| 2022 | 2021 | 2022 | 2021 | |||||||||||||
| Operating expenses: | ||||||||||||||||
| Research and development | $ | 23,118 | $ | 30,643 | $ | 60,917 | $ | 54,497 | ||||||||
| General and administrative | 9,867 | 10,129 | 21,336 | 18,365 | ||||||||||||
| Total operating expenses | 32,985 | 40,772 | 82,253 | 72,862 | ||||||||||||
| Loss from operations | (32,985 | ) | (40,772 | ) | (82,253 | ) | (72,862 | ) | ||||||||
| Other income (expense): | ||||||||||||||||
| Interest income | 27 | 40 | 41 | 106 | ||||||||||||
| Interest expense | (912 | ) | (194 | ) | (1,761 | ) | (194 | ) | ||||||||
| Other expense | (3 | ) | (11 | ) | ||||||||||||
| Total other expense, net | (888 | ) | (154 | ) | (1,731 | ) | (88 | ) | ||||||||
| Net loss | $ | (33,873 | ) | $ | (40,926 | ) | $ | (83,984 | ) | $ | (72,950 | ) | ||||
| Net loss per common share, basic and diluted | $ | (0.84 | ) | $ | (1.09 | ) | $ | (2.14 | ) | $ | (1.96 | ) | ||||
| Weighted average common shares outstanding, basic and diluted | 40,142,403 | 37,479,164 | 39,163,996 | 37,237,115 |
Taysha Gene Therapies, Inc.
Condensed Consolidated Balance Sheet Data
(in thousands, except share and per share data)
| June 30, 2022 | December 31, 2021 | |||||||
| ASSETS | ||||||||
| Current assets: | ||||||||
| Cash and cash equivalents | $ | 66,239 | $ | 149,103 | ||||
| Prepaid expenses and other current assets | 10,596 | 10,499 | ||||||
| Total current assets | 76,835 | 159,602 | ||||||
| Restricted cash | 2,637 | 2,637 | ||||||
| Deferred lease asset | 643 | 667 | ||||||
| Property, plant and equipment, net | 61,011 | 50,610 | ||||||
| Other non-current assets | 1,206 | 440 | ||||||
| Total assets | $ | 142,332 | $ | 213,956 | ||||
| LIABILITIES AND STOCKHOLDERS EQUITY | ||||||||
| Current liabilities | ||||||||
| Accounts payable | $ | 23,967 | $ | 21,763 | ||||
| Accrued expenses and other current liabilities | 18,986 | 29,983 | ||||||
| Total current liabilities | 42,953 | 51,746 | ||||||
| Build-to-suit lease liability | 25,609 | 25,900 | ||||||
| Term Loan, net | 37,580 | 37,192 | ||||||
| Other non-current liabilities | 3,480 | 3,735 | ||||||
| Total liabilities | 109,622 | 118,573 | ||||||
| Stockholders equity | ||||||||
| Preferred stock, $0.00001 par value per share; 10,000,000 shares authorized and no shares issued and outstanding as of June 30, 2022 and December 31, 2021 | ||||||||
| Common stock, $0.00001 par value per share; 200,000,000 shares authorized and 41,020,086 and 38,473,945 issued and outstanding as of June 30, 2022 and December 31, 2021, respectively | 1 | |||||||
| Additional paid-in capital | 352,342 | 331,032 | ||||||
| Accumulated deficit | (319,633 | ) | (235,649 | ) | ||||
| Total stockholders equity | 32,710 | 95,383 | ||||||
| Total liabilities and stockholders equity | $ | 142,332 | $ | 213,956 |
Chief Corporate Affairs Officer
Taysha Gene Therapies