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Healthcare - Biotechnology - NASDAQ - US
$ 8.32
2.4 %
$ 316 M
Market Cap
14.0
P/E
1. INTRINSIC VALUE

This DCF valuation model was last updated on Jun, 6, 2025.

The intrinsic value of one TRDA stock under the worst case scenario is HIDDEN Compared to the current market price of 8.32 USD, Entrada Therapeutics, Inc. is HIDDEN

This DCF valuation model was last updated on Jun, 6, 2025.

The intrinsic value of one TRDA stock under the base case scenario is HIDDEN Compared to the current market price of 8.32 USD, Entrada Therapeutics, Inc. is HIDDEN

This DCF valuation model was last updated on Jun, 6, 2025.

The intrinsic value of one TRDA stock under the best case scenario is HIDDEN Compared to the current market price of 8.32 USD, Entrada Therapeutics, Inc. is HIDDEN

2. FUNDAMENTAL ANALYSIS

Price Chart TRDA

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$20.0$20.0$18.0$18.0$16.0$16.0$14.0$14.0$12.0$12.0$10.0$10.0$8.0$8.0$6.0$6.015 Dec15 DecJan '25Jan '2515 Jan15 JanFeb '25Feb '2515 Feb15 FebMar '25Mar '2515 Mar15 MarApr '25Apr '2515 Apr15 AprMay '25May '2515 May15 MayJun '25Jun '25
FINANCIALS
211 M REVENUE
63.38%
47 M OPERATING INCOME
1586.75%
65.6 M NET INCOME
1081.69%
-41.6 M OPERATING CASH FLOW
-29.73%
-27.8 M INVESTING CASH FLOW
79.91%
103 M FINANCING CASH FLOW
389.44%
20.6 M REVENUE
-45.03%
-21.8 M OPERATING INCOME
-271.40%
-17.3 M NET INCOME
-1533.95%
-38.5 M OPERATING CASH FLOW
-21.84%
4.78 M INVESTING CASH FLOW
-91.04%
350 K FINANCING CASH FLOW
-75.04%
Balance Sheet Entrada Therapeutics, Inc.
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Current Assets 440 M
Cash & Short-Term Investments 420 M
Receivables 3.68 M
Other Current Assets 16.4 M
Non-Current Assets 86.3 M
Long-Term Investments 0
PP&E 82 M
Other Non-Current Assets 4.23 M
79.80 %3.11 %15.59 %Total Assets$526.3m
Current Liabilities 39.5 M
Accounts Payable 4.26 M
Short-Term Debt 7.56 M
Other Current Liabilities 27.7 M
Non-Current Liabilities 58.2 M
Long-Term Debt 103 M
Other Non-Current Liabilities -45.1 M
4.36 %7.74 %28.33 %105.79 %Total Liabilities$97.6m
EFFICIENCY
Earnings Waterfall Entrada Therapeutics, Inc.
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Revenue 211 M
Cost Of Revenue 0
Gross Profit 207 M
Operating Expenses 164 M
Operating Income 47 M
Other Expenses -18.6 M
Net Income 65.6 M
250m250m200m200m150m150m100m100m50m50m00211m0207m(164m)47m19m66mRevenueRevenueCost Of RevenueCost Of RevenueGross ProfitGross ProfitOperating ExpensesOperating ExpensesOperating IncomeOperating IncomeOther ExpensesOther ExpensesNet IncomeNet Income
RATIOS
98.21% GROSS MARGIN
98.21%
22.30% OPERATING MARGIN
22.30%
31.13% NET MARGIN
31.13%
15.31% ROE
15.31%
12.47% ROA
12.47%
9.39% ROIC
9.39%
FREE CASH FLOW ANALYSIS
Free Cash Flow Analysis Entrada Therapeutics, Inc.
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150m150m100m100m50m50m00(50m)(50m)(100m)(100m)202020202021202120222022202320232024202420252025
Net Income 65.6 M
Depreciation & Amortization 3.77 M
Capital Expenditures -3.16 M
Stock-Based Compensation 17.9 M
Change in Working Capital -119 M
Others -132 M
Free Cash Flow -44.7 M
3. WALL STREET ANALYSTS ESTIMATES
Wall Street Analysts Price Targets Entrada Therapeutics, Inc.
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Wall Street analysts predict an average 1-year price target for TRDA of $20.3 , with forecasts ranging from a low of $18 to a high of $23 .
TRDA Lowest Price Target Wall Street Target
18 USD 116.35%
TRDA Average Price Target Wall Street Target
20.3 USD 144.39%
TRDA Highest Price Target Wall Street Target
23 USD 176.44%
Price
Max Price Target
Min Price Target
Average Price Target
242422222020181816161414121210108866Jul '24Jul '24Aug '24Aug '24Oct '24Oct '24Nov '24Nov '2420252025Feb '25Feb '25Apr '25Apr '25Jun '25Jun '25Jul '25Jul '25Aug '25Aug '25Oct '25Oct '25Nov '25Nov '2520262026Feb '26Feb '26Apr '26Apr '26Jun '26Jun '26
4. DIVIDEND ANALYSIS
5. COMPETITION
slide 2 of 16
6. Ownership
Insider Ownership Entrada Therapeutics, Inc.
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Sold
0-3 MONTHS
19 K USD 1
3-6 MONTHS
0 USD 0
6-9 MONTHS
2.89 M USD 5
9-12 MONTHS
671 K USD 4
Bought
0 USD 0
0-3 MONTHS
0 USD 0
3-6 MONTHS
0 USD 0
6-9 MONTHS
337 USD 1
9-12 MONTHS
7. News
Entrada Therapeutics Appoints Maha Radhakrishnan, M.D., to its Board of Directors BOSTON, June 03, 2025 (GLOBE NEWSWIRE) -- Entrada Therapeutics, Inc. (Nasdaq: TRDA) today announced the appointment of Maha Radhakrishnan, M.D., to its Board of Directors. globenewswire.com - 2 weeks ago
Entrada Therapeutics Announces Inducement Grants Under Nasdaq Listing Rule 5635(c)(4) BOSTON, June 02, 2025 (GLOBE NEWSWIRE) -- Entrada Therapeutics, Inc. (Nasdaq: TRDA) today announced that the Company granted an aggregate of 23,820 restricted stock units (“RSUs”) to six newly-hired non-executive employees under the Company's 2025 Inducement Equity Plan (the “Inducement Plan”), effective as of June 1, 2025. The inducement grants were previously approved by the Compensation Committee of the Company's Board of Directors, as a material inducement to the new employees' entry into employment with the Company in accordance with Nasdaq Listing Rule 5635(c)(4). globenewswire.com - 2 weeks ago
Entrada Therapeutics Receives Authorization in the European Union to Initiate ELEVATE-45-201, a Phase 1/2 Multiple Ascending Dose Clinical Study of ENTR-601-45 in Patients Living with Duchenne Muscular Dystrophy Amenable to Exon 45 Skipping – Company on track to begin ELEVATE-45-201 in Q3 2025 – – Follows recently received Medicines and Healthcare Products Regulatory Agency authorization in the United Kingdom for ELEVATE-45-201 – BOSTON, May 28, 2025 (GLOBE NEWSWIRE) -- Entrada Therapeutics, Inc. (Nasdaq: TRDA) today announced it has received authorization from the Health Authorities and Ethics Committees of multiple countries under the European Union Clinical Trial Regulation (EU-CTR) to initiate ELEVATE-45-201, a Phase 1/2 multiple ascending dose (MAD) clinical study of ENTR-601-45 in patients living with Duchenne muscular dystrophy (DMD) who are amenable to exon 45 skipping. “ELEVATE-45-201 is the most advanced clinical study of a conjugated exon skipping therapy for individuals amenable to exon 45 skipping and offers the potential to address a large Duchenne subpopulation with significant unmet medical needs,” said Dipal Doshi, Chief Executive Officer at Entrada Therapeutics. globenewswire.com - 2 weeks ago
Entrada Therapeutics, Inc. (TRDA) Reports Q1 Loss, Tops Revenue Estimates Entrada Therapeutics, Inc. (TRDA) came out with a quarterly loss of $0.42 per share versus the Zacks Consensus Estimate of a loss of $0.78. This compares to earnings of $0.68 per share a year ago. zacks.com - 1 month ago
Entrada Therapeutics Reports First Quarter 2025 Financial Results – Receives regulatory authorization in the EU for ELEVATE-44-201, a Phase 1/2 MAD clinical study of ENTR-601-44 in patients living with Duchenne muscular dystrophy who are amenable to exon 44 skipping – – Company remains on track to initiate ELEVATE-44-201 and ELEVATE-45-201 in Q2 and Q3 2025, respectively – – Cash runway expected into Q2 2027 with $383 million in cash, cash equivalents and marketable securities as of March 31, 2025 – BOSTON, May 08, 2025 (GLOBE NEWSWIRE) -- Entrada Therapeutics, Inc. (Nasdaq: TRDA) today reported financial results for the first quarter ended March 31, 2025, and highlighted recent business updates. “We are excited to announce the first European Union regulatory clearance within our Duchenne franchise, with the authorization to initiate the ELEVATE-44-201 patient study across multiple countries. globenewswire.com - 1 month ago
Analysts Estimate Entrada Therapeutics, Inc. (TRDA) to Report a Decline in Earnings: What to Look Out for Entrada Therapeutics (TRDA) doesn't possess the right combination of the two key ingredients for a likely earnings beat in its upcoming report. Get prepared with the key expectations. zacks.com - 1 month ago
Entrada Therapeutics Receives Authorization in the United Kingdom to Initiate ELEVATE-45-201, a Phase 1/2 Multiple Ascending Dose Clinical Study of ENTR-601-45 in People Living with Duchenne Muscular Dystrophy Amenable to Exon 45 Skipping – Company on track to initiate ELEVATE-45-201 study in Q3 2025 – – ELEVATE-45 regulatory filings submitted in the EU, with regulatory review ongoing –  – ELEVATE-45 is the second of three novel exon skipping Duchenne programs the Company expects to progress into global clinical development in 2025 – BOSTON, March 24, 2025 (GLOBE NEWSWIRE) -- Entrada Therapeutics, Inc. (Nasdaq: TRDA) today announced it has received authorization from the United Kingdom's Medicines and Healthcare Products Regulatory Agency (MHRA) and Research Ethics Committee to initiate ELEVATE-45-201. ELEVATE-45-201 is a Phase 1/2 multiple ascending dose (MAD) clinical study to evaluate Entrada's investigational medicinal product ENTR-601-45 for the potential treatment of Duchenne muscular dystrophy (DMD) in patients with a confirmed mutation in the DMD gene amenable to exon 45 skipping. globenewswire.com - 2 months ago
Entrada Therapeutics, Inc. (TRDA) Surpasses Q4 Earnings and Revenue Estimates Entrada Therapeutics, Inc. (TRDA) came out with quarterly earnings of $0.03 per share, beating the Zacks Consensus Estimate of a loss of $0.66 per share. This compares to loss of $0.29 per share a year ago. zacks.com - 3 months ago
Entrada Therapeutics Reports Fourth Quarter and Full Year 2024 Financial Results – Received FDA authorization to initiate ELEVATE-44-102 in the U.S. – – Received MHRA authorization to initiate ELEVATE-44-201 in the U.K. – – Submitted regulatory filings to support global clinical studies for ENTR-601-44 in the EU, and ENTR-601-45 in the U.K. and EU – – Cash runway expected into Q2 2027 with $420 million in cash, cash equivalents and marketable securities as of December 31, 2024 – BOSTON, Feb. 27, 2025 (GLOBE NEWSWIRE) -- Entrada Therapeutics, Inc. (Nasdaq: TRDA) today reported financial results for the fourth quarter and full year ended December 31, 2024 and highlighted recent business updates. “We are thrilled to begin 2025 with significant momentum. globenewswire.com - 3 months ago
Entrada Therapeutics Announces FDA Removal of Clinical Hold on ENTR-601-44 – Receives FDA authorization to initiate ELEVATE-44-102, a Phase 1b multiple ascending dose clinical study of ENTR-601-44 in adults living with Duchenne muscular dystrophy – – Follows recently received Medicines and Healthcare Products Regulatory Agency authorization in the United Kingdom for ELEVATE-44-201 – – Expands global ELEVATE-44 clinical program to include pediatric, adult, ambulatory and non-ambulatory patients with Duchenne muscular dystrophy – BOSTON, Feb. 24, 2025 (GLOBE NEWSWIRE) -- Entrada Therapeutics, Inc. (Nasdaq: TRDA) today announced that the United States Food and Drug Administration (FDA) has lifted the clinical hold on ENTR-601-44 and provided authorization to initiate ELEVATE-44-102, a Phase 1b multiple ascending dose (MAD) clinical study of ENTR-601-44 for the potential treatment of Duchenne muscular dystrophy (DMD) in adult patients with a confirmed mutation in the DMD gene amenable to exon 44 skipping. The global ELEVATE-44 program, which includes the ELEVATE-44-102 study in the U.S. and ELEVATE-44-201 outside of the U.S., will cover a broad population of patients with DMD and support evaluation of ENTR-601-44 in patients with both early and advanced disease. globenewswire.com - 3 months ago
Entrada Therapeutics: Cash-Rich Innovator With Asymmetric Upside Entrada Therapeutics addresses intracellular drug delivery challenges with its Endosomal Escape Vehicle platform, positioning itself uniquely in the biotech sector. Strong financials with $449.3 million in reserves and strategic partnerships extend Entrada's runway into 2027, reducing near-term financing risks. ENTR-601-44, targeting Duchenne muscular dystrophy, is entering critical trials, with potential to validate the platform and drive significant market share. seekingalpha.com - 3 months ago
Entrada Therapeutics Receives Authorization in the United Kingdom to Initiate ELEVATE-44-201, a Phase 1/2 Multiple Ascending Dose Clinical Study of ENTR-601-44 in Patients Living with Duchenne Muscular Dystrophy – Company on track to initiate ELEVATE-44-201 in Q2 2025 – – ENTR-601-44 regulatory filings submitted in additional geographies including the U.S. and EU, with regulatory discussions ongoing – BOSTON, Feb. 03, 2025 (GLOBE NEWSWIRE) -- Entrada Therapeutics, Inc. (Nasdaq: TRDA) today announced it had received authorization from the United Kingdom's Medicines and Healthcare Products Regulatory Agency (MHRA) and Research Ethics Committee for its Clinical Trial of an Investigational Medicinal Product to initiate ELEVATE-44-201, a Phase 1/2 multiple ascending dose (MAD) clinical study of ENTR-601-44 for the potential treatment of Duchenne muscular dystrophy (DMD) in patients with a confirmed mutation in the DMD gene amenable to exon 44 skipping. “The clearance by the MHRA marks a new phase in Entrada's growth and, most importantly, moves us closer to realizing our commitment to families living with Duchenne muscular dystrophy,” said Dipal Doshi, Chief Executive Officer of Entrada Therapeutics. globenewswire.com - 4 months ago
8. Profile Summary

Entrada Therapeutics, Inc. TRDA

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COUNTRY US
INDUSTRY Biotechnology
MARKET CAP $ 316 M
Dividend Yield 0.00%
Description Entrada Therapeutics, Inc., a biotechnology company, develops endosomal escape vehicle (EEV) therapeutics for the treatment of multiple neuromuscular diseases. Its endosomal escape vehicle platform develops a portfolio of oligonucleotide, antibody, and enzyme-based programs. The company's lead product candidate is ENTR-601-44, which is in preclinical trail for the treatment of Duchenne muscular dystrophy and myotonic dystrophy type 1. It also engages in the development of EEV-PMO-CAG for the treatment of myotonic dystrophy type 1. The company was formerly known as CycloPorters, Inc. and changed its name to Entrada Therapeutics, Inc. in October 2017. Entrada Therapeutics, Inc. was incorporated in 2016 and is headquartered in Boston, Massachusetts.
Contact 6 Tide Street, Boston, MA, 02210 https://www.entradatx.com
IPO Date Oct. 29, 2021
Employees 183
Officers Mr. Nathan J. Dowden President & Chief Operating Officer Mr. Leo Qian Ph.D. Co-Founder & Vice President of Discovery Research Dr. Jared Cohen J.D., Ph.D. General Counsel Ms. Kerry Robert M.S. Senior Vice President of People Mr. Dipal Doshi Chief Executive Officer & Director Murali Mallem Vice President & Head of CMC Dr. Natarajan Sethuraman Ph.D. President of Research & Development Ms. Karla MacDonald Chief Corporate Affairs Officer Mr. Kevin Healy Ph.D. Senior Vice President of Regulatory Affairs Mr. Kory James Wentworth CPA Chief Financial Officer & Treasurer