Translate Bio Announces Third Quarter 2019 Financial Results and Reviews Recent Highlights
-- Advanced CF program with single-ascending dose (SAD) clinical data presentation and continued enrollment and dosing in multiple-ascending dose (MAD) portion of Phase 1/2 trial --
-- Prioritized and expanded discovery efforts on additional pulmonary disease targets --
-- Strengthened financial position to support ongoing clinical development of MRT5005 for the treatment of cystic fibrosis (CF) and additional pipeline programs into the first half of 2021 --
“In 2019, we have continued to make significant progress towards our goal of developing a new class of medicines utilizing our mRNA therapeutic platform. Building on the early positive data in our ongoing Phase 1/2 clinical trial in CF, we expanded our focus in pulmonary diseases and have also continued to build out critical operations across the Company including development of our delivery platform, growth of our manufacturing capabilities and preparations for future clinical development,” said Ronald Renaud, chief executive officer of
Third Quarter 2019 and Recent Highlights
- Presented early positive clinical data of MRT5005 at the
North American Cystic Fibrosis Conference: Described interim safety and tolerability results from the SAD portion of an ongoing, first-in-human Phase 1/2 clinical trial of MRT5005 in patients with CF. The MAD portion of the trial is ongoing with data expected in 2020.
- Expanded pulmonary disease focus with program pipeline update: Announced the prioritization of the development of pulmonary disease programs including the ongoing development of MRT5005 for the treatment of CF, as well as the evaluation of targets in additional pulmonary diseases.
- Entered into a strategic manufacturing agreement with
Albany Molecular Research, Inc.(AMRI): Announced a multi-year strategic manufacturing agreement with AMRI, a best-in-class, global clinical development manufacturing organization, in support of the planned expansion of the Company’s current Good Manufacturing Practices (cGMP) clinical mRNA manufacturing capabilities. The agreement provides Translate Biowith customized and dedicated manufacturing space for cGMP mRNA production for current and future programs.
$90Mpublic offering of common stock: Completed a public offering of 9,000,000 shares of common stock at a public offering price of $10.00per share, for gross proceeds of $90.0 million.
- MRT5005 (CF): Report results from the additional SAD dose group and MAD portion of Phase 1/2 clinical trial in 2020.
- Validate targets to support identification of development candidates for additional pulmonary diseases including primary ciliary dyskinesia, pulmonary arterial hypertension and idiopathic pulmonary fibrosis.
- The Company will present and host one-on-one meetings at the following investor conferences:
• Stifel 2019 Healthcare Conference,
November 19-20, 2019, New York, NY
Jefferies London Healthcare Conference, November 20-21, 2019, London, England
• Evercore ISI 2nd Annual
HealthCONx Conference, December 3-5, 2019, Boston, MA
- The Company will give a presentation entitled "Advancing the development of LNP-encapsulated mRNA therapeutics for pulmonary diseases" at the 7th International mRNA
Health Conferencetaking place November 11-12, 2019in Berlin, Germany.
Third Quarter 2019 Financial Results and Financial Guidance
Collaboration revenue was
Operating expenses for the three months ended
- Research and development expenses of
$17.3 millionduring the third quarter of 2019, compared to $12.9 millionfor the same period in 2018. The increase is primarily due to an increase in costs associated with the continued advancement of the CF program and continued development of MRT and vaccine discovery programs.
- General and administrative expenses of
$6.9 millionduring the third quarter of 2019, compared to $6.0 millionfor the same period in 2018. The increase is primarily due to an increase in personnel-related costs.
- An impairment charge of
$18.6 million representing the value of the indefinite-lived in-process research and development related to the ornithine transcarbamylase (OTC) deficiency program, the development of which the Company discontinued in the third quarter of 2019.
- Operating income of
$19.8 millionfor changes in the fair value of contingent consideration related to future potential milestone and earnout payment obligations. The operating income was attributed primarily to the decision to discontinue the OTC deficiency program, which resulted in the removal of $23.2 millionin contingent consideration liability related to the OTC deficiency program, largely offset by an increase in the fair value of the contingent consideration liability related to the CF program due to its continued progress and the time value of money due to passage of time.
Translate Bio is a clinical-stage mRNA therapeutics company developing a new class of potentially transformative medicines to treat diseases caused by protein or gene dysfunction. The Company’s MRT platform is designed to develop product candidates that deliver mRNA carrying instructions to produce intracellular, transmembrane and secreted proteins for therapeutic benefit. Translate Bio is primarily focused on applying its MRT platform to treat pulmonary diseases caused by insufficient protein production or where production of proteins can modify disease. The Company also believes its technology is applicable to a broad range of diseases, including diseases that affect the liver, eye and central nervous system. Additionally, the MRT platform may be applied to various classes of treatments, such as therapeutic antibodies or vaccines in areas such as infectious disease and oncology. Translate Bio’s lead program is being developed as a treatment for cystic fibrosis (CF) and is in an ongoing Phase 1/2 clinical trial. For more information about the Company, please visit www.translate.bio or on Twitter at @TranslateBio.
Cautionary Note Regarding Forward-Looking Statements
This press release contains forward-looking statements within the meaning of The Private Securities Litigation Reform Act of 1995. Such forward-looking statements include, but are not limited to, those regarding: the potential for MRT5005 to address the underlying cause of CF and benefit patients; Translate Bio’s plans to report data from the additional SAD dose group and MAD part of the Phase 1/2 clinical trial of MRT5005 in 2020; Translate Bio’s plans to advance its pipeline of mRNA therapeutics and validate targets for additional pulmonary diseases; the period in which Translate Bio expects that its existing cash, cash equivalents and investments will enable it to fund its operations; Translate Bio’s beliefs regarding the broad applicability of its MRT platform; and Translate Bio’s plans, strategies and prospects for its business, including its lead development programs. The words “anticipate,” “believe,” “continue,” “could,” “estimate,” “expect,” “forward”, “intend,” “may,” “plan,” “potential,” “predict,” “project,” “should,” “target,” “would” and similar expressions are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words. Such statements are subject to numerous important factors, risks and uncertainties that may cause actual events or results to differ materially from current expectations and beliefs, including but not limited to: Translate Bio’s ability to advance the development of its platform and programs under the timelines it projects, demonstrate the requisite safety and efficacy of its product candidates and replicate in clinical trials any positive findings from preclinical studies; the content and timing of decisions made by the U.S. Food and Drug Administration, other regulatory authorities and investigational review boards at clinical trial sites, including decisions as it relates to ongoing and planned clinical trials; Translate Bio’s ability to obtain, maintain and enforce necessary patent and other intellectual property protection; the availability of significant cash required to fund operations; competitive factors; general economic and market conditions and other important risk factors set forth under the caption “Risk Factors” in Translate Bio’s Quarterly Report on Form 10-Q for the quarterly period ended
|TRANSLATE BIO, INC.|
|CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS|
|Three Months Ended September 30,||Nine Months Ended September 30,|
|Research and development||17,295||12,933||51,343||40,854|
|General and administrative||6,881||5,957||21,284||16,726|
|Change in fair value of contingent consideration||(19,834||)||26,829||(3,243||)||39,589|
|Impairment of intangible asset||18,559||—||18,559||—|
|Total operating expenses||22,901||45,719||87,943||97,169|
|Loss from operations||(21,635||)||(45,481||)||(84,029||)||(96,931||)|
|Other income (expense):|
|Total other income (expense), net||408||311||1,286||447|
|Loss before benefit from income taxes||(21,227||)||(45,170||)||(82,743||)||(96,484||)|
|Benefit from income taxes||—||2,524||486||5,126|
|TRANSLATE BIO, INC.|
|CONDENSED CONSOLIDATED BALANCE SHEETS|
|Cash and cash equivalents||$||98,930||$||55,199|
|Prepaid expenses and other current assets||6,648||4,474|
|Total current assets||217,761||149,602|
|Property and equipment, net||10,680||10,245|
|Right-of-use assets, net||10,527||—|
|Intangible assets, net||86,695||106,445|
|Other long-term assets||2,492||—|
|Liabilities and Stockholders' Equity|
|Current portion of deferred revenue||12,603||2,572|
|Current portion of operating lease liability||489||—|
|Total current liabilities||25,266||14,287|
|Long-term portion of contingent consideration||100,399||103,642|
|Deferred revenue, net of current portion||30,046||41,841|
|Deferred tax liabilities||—||481|
|Operating lease liability, net of current portion||12,230||—|
|Additional paid-in capital||509,294||371,257|
|Accumulated other comprehensive income||679||196|
|Total stockholders' equity||181,573||125,295|
|Total liabilities and stockholders' equity||$||349,514||$||287,651|
Source: Translate Bio, Inc.