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MeiraGTx Reports Second Quarter 2023 Financial and Operational Results - Phase 3 LUMEOS clinical trial of botaretigene sparoparvovec (bota-vec, formerly AAV-RPGR) for the treatment of X-linked retinitis pigmentosa (XLRP)

Key Takeaway: MeiraGTx Holdings plc reported its financial and operational results for Q2 2023, highlighting advancements in their clinical programs and technologies. The positive outcomes in the completed AQUAx Phase 1 study and ongoing Phase 3 LUMEOS trial for bota-vec are notable. The company has also secured a commercial QC testing license for its manufacturing facility in Ireland, allowing it to expand its operational capabilities. However, the company experienced a decrease in license revenue and an increase in expenses, which could pose financial challenges.

Market Sentiment Analysis

POSITIVE FACTORS

  • Progress in clinical trials with positive data from the AQUAx Phase 1 study.
  • Successful enrollment and progress in the Phase 3 LUMEOS trial for XLRP.
  • The company has received a commercial QC testing license for its manufacturing facility in Ireland, enhancing operational capabilities.

CONCERNS & RISKS

  • A decrease in license revenue compared to the same quarter in the previous year.
  • Increased general and administrative expenses were noted, raising concerns over operational costs.

Full Press Release Details

MeiraGTx Reports Second Quarter 2023 Financial and Operational Results
LONDON and NEW YORK, August 10, 2023 (GLOBE NEWSWIRE) -- MeiraGTx Holdings plc (Nasdaq: MGTX), a vertically integrated, clinical stage gene therapy company, today announced financial and operational results for the second quarter ended June 30, 2023, and provided a corporate update.
"Progress across our programs and infrastructure continues to be extremely impressive," said Alexandria Forbes, Ph.D., president and chief executive officer of MeiraGTx. "This includes further advancement of our three lead clinical programs, our riboswitch gene regulation technology platform, and our manufacturing platform. This quarter, we announced positive data from the completed AQUAx Phase 1 study, demonstrating clinically meaningful improvements in long term xerostomia patients, and we are currently enrolling and treating patients in our Phase 2 trial. In the Phase 3 LUMEOS trial of bota-vec for the treatment of XLRP, we have now surpassed the enrollment target and expect a BLA submission next year. In addition, we presented unprecedented preclinical data from our novel gene regulation platform at the ASGCT Annual and ASGCT Spotlight on Immuno-oncology meetings. We are particularly excited by our groundbreaking RiboCAR technology. RiboCAR enables precise and reversible regulation of CAR expression in response to small molecule inducers, with the regulated CAR-T showing increased activity and durability compared to CAR-T with constitutively active CAR, as well as significant implications for safety. We are excited to continue this work with leaders in the field in moving RiboCAR towards the clinic, particularly in the treatment of solid tumors where we believe RiboCAR's benefits have the potential to transform patient outcomes."
Dr. Forbes continued, "We continue to build on our unique end-to-end manufacturing capabilities with a commercial QC testing license for our state-of-the-art manufacturing facility in Shannon, Ireland. This is the first commercial license for a gene therapy facility in Ireland. This authorization allows us to accelerate the development of our pipeline and serve as a reliable QC testing facility for advanced therapies on a global scale, and provides the opportunity to add additional revenue from potential partners."
Recent Development Highlights and Anticipated Milestones
Bota-vec for the Treatment of XLRP:
AAV-hAQP1 for the Treatment of Grade 2/3 Radiation-Induced Xerostomia:
Wholly-Owned Gene Therapy Manufacturing Facility in Shannon, Ireland has Received Commercial MIA Authorization for QC Testing
AAV-GAD for the Treatment of Parkinson's Disease:
Riboswitch Gene Regulation Platform & Vector Engineering:
For more information related to our clinical trials, please visit www.clinicaltrials.gov
As of June 30, 2023, MeiraGTx had cash and cash equivalents of approximately $92.8 million, as well as approximately $32.7 million in receivables due from Janssen. The Company believes that with such funds, as well as anticipated milestones from Janssen, it will have sufficient capital to fund operating expenses and capital expenditure requirements into the second quarter of 2025.
Cash and cash equivalents were $92.8 million as of June 30, 2023, compared to $115.5 million as of December 31, 2022.
License revenue was $3.5 million for the quarter ended June 30, 2023, compared to $10.8 million for the quarter ended June 30, 2022. This decrease represents decreased amortization of the $100.0 million upfront payment as well as decreased amortization of the $30.0 million milestone payment received in connection with the Janssen collaboration.
General and administrative expenses were $12.4 million for the three months ended June 30, 2023, compared to $10.5 million for the three months ended June 30, 2022. The increase of $1.9 million was primarily due to an increase in legal and accounting fees, payroll and payroll-related
costs, share-based compensation and other office related costs. These increases were partially offset by decreases in insurance costs and consulting fees.
Research and development expenses for the three months ended June 30, 2023, were $19.9 million, compared to $24.0 million for the three months ended June 30, 2022. The decrease of $4.1 million was primarily due to a decrease in expenses related to our preclinical programs primarily due to the timing of expenses in our gene regulation program, manufacturing costs related to lower production volumes, other research and development expenses primarily due to a decrease in share-based compensation, and an increase in research funding provided under our Janssen collaboration primarily due to the increase in expenses incurred related to our program for bota-vec for the treatment of XLRP. These decreases were partially offset by an increase in clinical trial expenses primarily due to an increase in expenses related to our Phase 3 LUMEOS clinical trial of bota-vec and our expanded Phase 1 clinical trial and our Phase 2 clinical trial for AAV-hAQP1.
Foreign currency gain was $1.9 million for the three months ended June 30, 2023, compared to a loss of $10.4 million for the three months ended June 30, 2022. The change of $12.3 million was primarily due to an unrealized gain on the quarterly valuation of intercompany payables and receivables due to the weakening of the U.S. dollar against the pound sterling and euro during the three months ended June 30, 2023.
Net loss attributable to ordinary shareholders for the quarter ended June 30, 2023 was $29.6 million, or $0.53 basic and diluted net loss per ordinary share, compared to a net loss attributable to ordinary shareholders of $34.0 million, or $0.76 basic and diluted net loss per ordinary share for the quarter ended June 30, 2022.
MeiraGTx (Nasdaq: MGTX) is a vertically integrated, clinical-stage gene therapy company with six programs in clinical development and a broad pipeline of preclinical and research programs. MeiraGTx has core capabilities in viral vector design and optimization and gene therapy manufacturing, and a transformative gene regulation platform technology that allows precise, dose responsive control of gene expression by oral small molecules with dynamic range that can exceed 5000-fold. Led by an experienced management team, MeiraGTx has taken a portfolio approach by licensing, acquiring, and developing technologies that give depth across both product candidates and indications. MeiraGTx's initial focus is on three distinct areas of unmet medical need: ocular diseases, including both inherited retinal diseases as well as large degenerative ocular diseases, neurodegenerative diseases and severe forms of xerostomia. Though initially focusing on the eye, central nervous system, and salivary gland, MeiraGTx plans to expand its focus to develop additional gene therapy treatments for patients suffering from a range of serious diseases.
For more information, please visit www.meiragtx.com
Forward Looking Statement
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. All statements contained in this press release that do not relate to matters of historical fact should be considered forward-looking statements,
including, without limitation, statements regarding our product candidate development and anticipated milestones regarding our pre-clinical and clinical data, reporting of such data and the timing of results of data and regulatory matters, as well as statements that include the words "expect," "will," "intend," "plan," "believe," "project," "forecast," "estimate," "may," "could," "should," "would," "continue," "anticipate" and similar statements of a future or forward-looking nature. These forward-looking statements are based on management's current expectations. These statements are neither promises nor guarantees, but involve known and unknown risks, uncertainties and other important factors that may cause actual results, performance or achievements to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements, including, but not limited to, our incurrence of significant losses; any inability to achieve or maintain profitability, raise additional capital, repay our debt obligations, identify additional and develop existing product candidates, successfully execute strategic priorities, bring product candidates to market, expansion of our manufacturing facilities and processes, successfully enroll patients in and complete clinical trials, accurately predict growth assumptions, recognize benefits of any orphan drug designations, retain key personnel or attract qualified employees, or incur expected levels of operating expenses; the impact of the COVID-19 pandemic on the status, enrollment, timing and results of our clinical trials and on our business, results of operations and financial condition; failure of early data to predict eventual outcomes; failure to obtain FDA or other regulatory approval for product candidates within expected time frames or at all; the novel nature and impact of negative public opinion of gene therapy; failure to comply with ongoing regulatory obligations; contamination or shortage of raw materials or other manufacturing issues; changes in healthcare laws; risks associated with our international operations; significant competition in the pharmaceutical and biotechnology industries; dependence on third parties; risks related to intellectual property; changes in tax policy or treatment; our ability to utilize our loss and tax credit carryforwards; litigation risks; and the other important factors discussed under the caption "Risk Factors" in our Quarterly Report on Form 10-Q for the quarter ended June 30, 2023, as such factors may be updated from time to time in our other filings with the SEC, which are accessible on the SEC's website at www.sec.gov. These and other important factors could cause actual results to differ materially from those indicated by the forward-looking statements made in this press release. Any such forward-looking statements represent management's estimates as of the date of this press release. While we may elect to update such forward-looking statements at some point in the future, unless required by law, we disclaim any obligation to do so, even if subsequent events cause our views to change. Thus, one should not assume that our silence over time means that actual events are bearing out as expressed or implied in such forward-looking statements. These forward-looking statements should not be relied upon as representing our views as of any date subsequent to the date of this press release.
LifeSci Communications
MEIRAGTX HOLDINGS PLC AND SUBSIDIARIES
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS AND COMPREHENSIVE LOSS
(in thousands, except share and per share amounts)
For the Three-Month Period Ended June 30, For the Six-Month Period Ended June 30,
2023 2022 2023 2022
License revenue - related party $ 3,540 $ 10,759 $ 6,874 $ 16,392
Operating expenses:
General and administrative 12,388 10,518 25,160 21,786
Research and development 19,937 23,999 42,259 47,098
Total operating expenses 32,325 34,517 67,419 68,884
Loss from operations (28,785) (23,758) (60,545) (52,492)
Other non-operating income (expense):
Foreign currency gain (loss) 1,905 (10,426) 5,762 (13,073)
Interest income 655 41 1,200 57
Interest expense (3,355) (82) (6,415) (159)
Fair value adjustment (1) 252 53 649
Net loss (29,581) (33,973) (59,945) (65,018)
Other comprehensive (loss) income:
Foreign currency translation (loss) gain (2,541) 7,357 (4,894) 9,290
Comprehensive loss $ (32,122) $ (26,616) $ (64,839) $ (55,728)
Net loss $ (29,581) $ (33,973) $ (59,945) $ (65,018)
Basic and diluted net loss per ordinary share $ (0.53) $ (0.76) $ (1.15) $ (1.46)
Weighted-average number of ordinary shares outstanding 55,349,534 44,668,240 52,012,382 44,585,239
MEIRAGTX HOLDINGS PLC AND SUBSIDIARIES
CONDENSED CONSOLIDATED BALANCE SHEETS
(in thousands, except share and per share amounts)
June 30, December 31,
2023 2022
ASSETS
CURRENT ASSETS:
Cash and cash equivalents $ 92,773 $ 115,516
Accounts receivable - related party 32,690 21,334
Prepaid expenses 8,108 8,133
Tax incentive receivable 8,026 7,689
Other current assets 1,547 1,667
Total Current Assets 143,144 154,339
Property, plant and equipment, net 114,004 109,266
Intangible assets, net 1,252 1,335
In-process research and development 753 742
Other assets 1,465 1,402
Equity method and other investments 6,326 6,326
Right-of-use assets - operating leases, net 18,693 20,109
Right-of-use assets - finance leases, net 24,626 24,718
TOTAL ASSETS $ 310,263 $ 318,237
LIABILITIES AND SHAREHOLDERS' EQUITY
CURRENT LIABILITIES:
Accounts payable $ 28,497 $ 16,616
Accrued expenses 24,889 39,818
Lease obligations, current 4,126 3,884
Deferred revenue - related party, current 12,058 15,123
Other current liabilities 2,233 6,631
Total Current Liabilities 71,803 82,072
Deferred revenue - related party 25,364 27,436
Lease obligations 15,508 17,331
Asset retirement obligations 2,301 2,179
Deferred income tax liability 189 186
Note payable, net 71,571 71,033
Other long-term liabilities - 262
TOTAL LIABILITIES 186,736 200,499
COMMITMENTS AND CONTINGENCIES (Note 10)
SHAREHOLDERS' EQUITY:
Ordinary Shares, $0.00003881 par value, 1,288,327,750 authorized, 59,535,314 and 48,477,209 shares issued and outstanding at June 30, 2023 and December 31, 2022, respectively 2 2
Capital in excess of par value 652,521 581,893
Accumulated other comprehensive income 1,153 6,047
Accumulated deficit (530,149) (470,204)
Total Shareholders' Equity 123,527 117,738
TOTAL LIABILITIES AND SHAREHOLDERS' EQUITY $ 310,263 $ 318,237

Frequently Asked Questions

What recent progress did MeiraGTx report in clinical programs?

MeiraGTx announced advancements in three lead clinical programs and positive data from the completed AQUAx Phase 1 study.

What technology is MeiraGTx developing for gene regulation?

MeiraGTx is developing a novel riboswitch gene regulation technology platform, including RiboCAR.

What is the financial status of MeiraGTx as of June 2023?

As of June 30, 2023, MeiraGTx had approximately $92.8 million in cash, and expects funds to last into Q2 2025.

How did MeiraGTx's net loss change compared to last year?

MeiraGTx reported a net loss of $29.6 million for Q2 2023, down from $34.0 million in Q2 2022.

What is the significance of the facility in Shannon, Ireland?

The facility has received a commercial QC testing license, enhancing MeiraGTx’s manufacturing capabilities.

Last updated: Aug 10, 2023