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Entrada Therapeutics Reports First Quarter 2022 Financial Results Second clinical candidate, ENTR-701, announced for the potential treatment of myotonic dystrophy type 1 On track to submit Investigational New Drug applic

Key Takeaway: Entrada Therapeutics Reports First Quarter 2022 Second clinical candidate, ENTR-701, announced for the potential treatment of myotonic dystrophy type 1 On track to submit Investigational New Drug application to the U.S. Food and Drug Administration for ENTR-601-44 targeting D

Full Press Release Details

Entrada Therapeutics Reports First Quarter 2022
Second clinical candidate, ENTR-701, announced
for the potential treatment of myotonic dystrophy type 1
On track to submit Investigational New Drug
application to the U.S. Food and Drug Administration for ENTR-601-44 targeting Duchenne muscular dystrophy in Q4 2022
$263.9 million in cash, cash equivalents and
marketable securities as of March 31, 2022 to advance pipeline of Endosomal Escape Vehicle (EEV ) therapeutic candidates
BOSTON, May 12, 2022 (GLOBE NEWSWIRE) -- Entrada Therapeutics, Inc.
(Nasdaq: TRDA), a biopharmaceutical company aiming to transform the lives of patients by establishing intracellular Endosomal Escape Vehicle
(EEV ) therapeutics as a new class of medicines, today reported financial results for the first quarter ended March 31, 2022 and
highlighted recent business updates.
"In the first quarter of 2022, we continued to make significant
progress in advancing our growing pipeline of EEV therapeutic candidates," said Dipal Doshi, President and Chief Executive Officer
of Entrada. "We reported encouraging new data from preclinical studies on our lead neuromuscular candidate, ENTR-601-44, for patients
with Duchenne muscular dystrophy who are exon 44 skipping amenable, as well as from our myotonic dystrophy type 1 program. Just this month,
we were excited to present additional preclinical data at TIDES USA that reinforce our conviction in developing ENTR-701, our newly announced
clinical candidate for myotonic dystrophy type 1, one of the most predominant rare neuromuscular diseases for which there are currently
no approved therapies."
Recent Corporate Highlights
Upcoming Scientific Meetings
Entrada plans to present at two additional scientific meetings in May
2022. Presentations from both meetings will be available on the Publications & Conferences section of the Entrada website following
Title: Development of Endosomal Escape Vehicles to
Enhance the Intracellular Delivery of Oligonucleotides
Session: Oligonucleotide Therapeutics I
Presenter: Leo Ziqing Qian, PhD, Co-Founder &
Vice President, Discovery Research of Entrada
Date & Time: Monday, May 16 from 5:30 -
Location: Virtual and in-person in Washington, D.C.
Session: Exon Skipping and Read Through Agents Panel
Presenter: Nerissa Kreher, MD, Chief Medical Officer
Date & Time: Monday, May 28 from 1:55 -
Location: Virtual and in-person in Orlando, FL
First Quarter 2022 Financial Results
Cash Position: Cash, cash equivalents and marketable securities
were $263.9 million as of March 31, 2022, compared to $291.1 million as of December 31, 2021. Based on current operating plans, Entrada
expects its existing cash, cash equivalents and marketable securities will enable the company to fund its operating expenses and capital
expenditure requirements into the second half of 2024.
Research & Development (R&D) Expenses: R&D expenses
for the first quarter of 2022 were $15.7 million, compared to $6.2 million for the same period in 2021. This increase was primarily due
to additional investment in preclinical studies to support future clinical trials, enhanced facility and equipment-related investments
and higher personnel costs (including non-cash stock-based compensation).
General & Administrative (G&A) Expenses: G&A expenses
for the first quarter of 2022 were $6.4 million, compared to $2.2 million for the same period in 2021. This increase was primarily due
to higher personnel costs (including non-cash stock-based compensation), legal and other professional fees, and facilities costs.
Net Loss: Net loss for the first quarter of 2022 was $21.7 million,
compared to $8.4 million for the same period of 2021.
About Entrada Therapeutics
Entrada Therapeutics is a biopharmaceutical
company aiming to transform the lives of patients by establishing a new class of medicines, Endosomal Escape Vehicle (EEV ) therapeutics,
to engage intracellular targets that have long been considered inaccessible and undruggable. The Company's EEV therapeutics are
designed to enable the efficient intracellular delivery of a wide range of therapeutics into a variety of organs and tissues with an improved
therapeutic index. Through its proprietary, highly versatile and modular EEV platform, Entrada is building a robust development portfolio
of oligonucleotide-, antibody- and enzyme-based programs for the potential treatment of neuromuscular diseases, immunology, oncology and
diseases of the central nervous system. The Company's lead oligonucleotide programs include ENTR-601-44 targeting Duchenne muscular
dystrophy (DMD) and ENTR-701 targeting myotonic dystrophy type 1 (DM1).
For more information about Entrada, please
Forward-Looking Statements
This press release contains forward-looking statements that involve
substantial risks and uncertainties. All statements, other than statements of historical facts, contained in this press release, including
statements regarding Entrada's strategy, future operations, prospects and plans, objectives of management, the continued development
of ENTR-601-44, including the Investigational New Drug (IND) application-enabling studies, the timing of Entrada's planned regulatory
filings regarding its development programs, expectations regarding the preclinical data of ENTR-601-44 and ENTR-701 and the related potential
for development, the progression of early-stage oligonucleotide, antibody and enzyme-based programs into clinical development, the continued
development and advancement of ENTR-601-44 for the treatment of DMD and ENTR-701 for the treatment of DM1, the potential therapeutic benefits
of its EEV candidates, and the sufficiency of its cash resources, constitute forward-looking statements within the meaning of The Private
Securities Litigation Reform Act of 1995. The words "anticipate," "believe," "continue," "could,"
"estimate," "expect," "intend," "may," "might," "objective," "ongoing,"
"plan," "predict," "project," "potential," "should," or "would,"
or the negative of these terms, or other comparable terminology are intended to identify forward-looking statements, although not all
forward-looking statements contain these identifying words. Entrada may not actually achieve the plans, intentions or expectations disclosed
in these forward-looking statements, and you should not place undue reliance on these forward-looking statements. Actual results or events
could differ materially from the plans, intentions and expectations disclosed in these forward-looking statements as a result of various
important factors, including: uncertainties inherent in the identification and development of product candidates, including the conduct
of research activities and the initiation and completion of preclinical studies and clinical trials; uncertainties as to the availability
and timing of results from preclinical studies; the timing of and Entrada's ability to submit and obtain regulatory clearance for
IND applications and initiate clinical trials; whether results from preclinical studies will be predictive of the results of later preclinical
studies and clinical trials; whether Entrada's cash resources will be sufficient to fund the Company's foreseeable and unforeseeable
operating expenses and capital expenditure requirements; uncertainties associated with the impact of the ongoing COVID-19 pandemic on
Entrada's business and operations; as well as the risks and uncertainties identified in Entrada's filings with the Securities
and Exchange Commission (SEC), including the Company's most recent Form 10-K and in subsequent filings Entrada may make with the
SEC. In addition, the forward-looking statements included in this press release represent Entrada's views as of the date of this
press release. Entrada anticipates that subsequent events and developments will cause its views to change. However, while Entrada may
elect to update these forward-looking statements at some point in the future, it specifically disclaims any obligation to do so. These
forward-looking statements should not be relied upon as representing Entrada's views as of any date subsequent to the date of this
ENTRADA THERAPEUTICS, INC.
Condensed Consolidated Statements of Operations
(In thousands, except share and per share amounts)
Three Months Ended March 31,
2022 2021
Operating expenses:
Research and development $ 15,718 $ 6,223
General and administrative 6,433 2,170
Total operating expenses 22,151 8,393
Loss from operations (22,151 ) (8,393 )
Other income:
Interest and other income, net 480 13
Total other income, net 480 13
Net loss $ (21,671 ) $ (8,380 )
Net loss per share attributable to common stockholders, basic and diluted $ (0.69 ) $ (6.67 )
Weighted-average common shares outstanding, basic and diluted 31,246,916 1,256,487
ENTRADA THERAPEUTICS, INC.
Condensed Consolidated Balance Sheet Data (Unaudited)
March 31, 2022 December 31, 2021
Cash and cash equivalents $ 84,640 $ 291,064
Marketable securities 179,262 -
Total assets 316,702 305,833
Total liabilities 39,311 7,115
Total stockholders' equity 277,391 298,718
Investor and Media Contact
VP, Corporate Communications and Investor Relations
Last updated: May 12, 2022