Entrada Therapeutics, Inc.

Entrada Therapeutics, Inc.

TRDA
Entrada Therapeutics, Inc.US flagNASDAQ Global Market
6.46
USD
+0.12
- -
250.78MMarket Cap
2019 Y
2020 Y
2021 Y
2022 Y
2023 Y
2024 Y
2025 Y
TTM
Revenue per Share
- -
- -
- -
- -
3.9
5.65
0.61
0.14
Basic EPS, GAAP
-0.4
-1.3
-8.16
-3.02
-0.2
1.76
-3.47
-4
Free Cash Flow per Basic Share
-0.89
-1.36
-8.85
-3.09
4.06
-1.2
-3.13
-3.17
Dividend per Share
- -
- -
- -
- -
- -
- -
- -
- -
Book Value per Share
-1.24
-2.08
-14.94
-6.02
-5.9
-3.47
-6.6
-7.53
Tangible Book Value per Share
-1.2
-2.03
47.66
6.79
7.33
11.49
7.4
6.52
Basic Weighted Avg Shares
13
20
6
31
33
37
41
42
Sales/Revenue/Turnover
- -
- -
- -
- -
129
211
25
6
Operating Margin (%)
- -
- -
- -
- -
-2.45
22.3
-621.13
-3,109.29
Depreciation Expense
- -
- -
1
2
3
4
4
4
Net Income, GAAP
-5
-27
-51
-95
-7
66
-144
-166
Effective Tax Rate (%)
- -
- -
- -
- -
155.45
1.29
- -
- -
Profit Margin (%)
- -
- -
- -
- -
-5.18
31.13
-565.48
-2,895.05
Working Capital
16
37
292
188
211
401
282
248
LT Debt
- -
- -
- -
18
60
52
47
45
Total Equity
-16
-41
299
213
242
429
306
271
Return on Invested Capital (%)
- -
- -
- -
- -
0.63
11.56
- -
- -
Return on Capital (%)
- -
- -
- -
- -
- -
- -
- -
- -
Return on Common Equity (%)
- -
- -
- -
- -
- -
- -
- -
- -

Capital Structure

FRC

in mil. unless spec.
Sep'25
Dec'25
Mar'26
ST Debt
4
4
- -
LT Borrowings
- -
- -
- -
LT Finance Leases
48
47
45
Preferred Equity and Hybrid Capital
- -
- -
- -
Shares Outstanding
38
38
39
Market Capitalization
239
425
524

Working Capital

FRC

in mil. unless spec.
Sep'25
Dec'25
Mar'26
Total Current Assets
338
306
267
Cash, Cash Equivalents & STI
327
296
76
Accounts Receivable, Net
- -
- -
- -
Inventories
- -
- -
- -
Total Current Liabilities
24
24
19
Payables & Accruals
12
11
- -
ST Debt
4
4
- -
Deferred Revenue
- -
- -
- -

Growth Rates

FRC

in mil. unless spec.

(avg. rate of change)

10 years
5 years
1 year
Total Equity
- -
-157.3%
-28.59%
Free Cash Flow
- -
-1.85%
189.73%
Net Income, GAAP
- -
-263.17%
-319.04%
Sales/Revenue/Turnover
- -
- -
-87.94%
Total Cash Common Dividend
- -
- -
- -

Quarterly Revenue

FRC

in mil. unless spec.

Year

Q1
Q2
Q3
Q4
FY
2024
59
95
20
37
211
2025
21
2
2
1
25
2026
1
- -
- -
- -
- -

Quarterly Earnings Per Share

FRC

in mil. unless spec.

Year

Q1
Q2
Q3
Q4
FY
2024
0.7
1.61
-0.35
0.03
1.76
2025
-0.42
-1.04
-1.06
-0.94
-3.47
2026
-0.95
- -
- -
- -
- -

Quarterly Dividends Per Share

FRC

in mil. unless spec.

Year

Q1
Q2
Q3
Q4
FY
2024
- -
- -
- -
- -
- -
2025
- -
- -
- -
- -
- -
2026
- -
- -
- -
- -
- -

Company Description

APIChatGPT
CEO
Dipal Doshi
Full Time Employees
152
Sector
Healthcare
Industry
Biotechnology
Address
One Design Center Place Boston MA United States of America 02210
IPO Date
Oct 29, 2021
Business
Entrada Therapeutics, Inc. is a clinical-stage biopharmaceutical company specializing in the development of a new class of medicines based on its proprietary Endosomal Escape Vehicle (EEV™) platform. The company focuses on enabling the intracellular delivery of therapeutics that target previously inaccessible intracellular pathways. Its core product pipeline features EEV-conjugated oligonucleotide therapeutics designed primarily for neuromuscular diseases, including Duchenne muscular dystrophy (DMD), with lead programs ENTR-601-44 and ENTR-601-45 targeting exon 44 and exon 45 skipping amenable DMD patients, respectively. The company also develops programs targeting myotonic dystrophy type 1 (ENTR-701), mitochondrial neurogastrointestinal encephalomyopathy, ocular diseases, immunology, oncology, and central nervous system disorders. These products leverage EEV technology to deliver RNA-, antibody-, and enzyme-based therapies across multiple organs and tissues. Founded in 2017 and headquartered in Boston, Massachusetts, Entrada Therapeutics operates globally with a focus on advancing its therapeutic pipeline through clinical trials and strategic partnerships. Recent major developments include authorization by regulatory authorities in the United Kingdom and the European Union to initiate Phase 1/2 multiple ascending dose clinical studies for ENTR-601-44 and ENTR-601-45, marking significant clinical advancement in the Duchenne muscular dystrophy franchise. The company has also achieved key milestones under its global collaboration with Vertex Pharmaceuticals on VX-670, a clinical-stage program for myotonic dystrophy type 1, and maintains a strategic partnership with Pierrepont Therapeutics focused on mitochondrial diseases. Collaboration revenue reached $210.8 million in 2024, reflecting these strategic alliances and clinical progress. Entrada is expanding its Duchenne franchise with additional planned filings for exon 50 targeting therapies expected to further broaden patient reach. Entrada Therapeutics is advancing robust clinical and preclinical development programs leveraging its modular EEV platform to address high unmet medical needs in rare and serious diseases. Its unique approach aims to transform treatment paradigms by delivering challenging intracellular therapies with improved efficacy and therapeutic index. The company remains focused on the development and commercialization potential of these novel therapeutics across neuromuscular, ocular, immunological, metabolic, and oncology segments, supported by a strong financial position and a growing network of strategic collaborations. This profile reflects the latest information as of late 2025, highlighting Entrada Therapeutics’ leadership in innovative intracellular drug delivery technology and its progression into clinical development phases for multiple rare diseases.

Company News

APIChatGPT
  • Entrada Therapeutics, Inc. (TRDA) Presents at Goldman Sachs 47th Annual Global Healthcare Conference 2026 Transcript

  • INVESTOR ALERT: Pomerantz Law Firm Investigates Claims On Behalf of Investors of Entrada Therapeutics, Inc. - TRDA

  • INVESTOR ALERT: Pomerantz Law Firm Investigates Claims On Behalf of Investors of Entrada Therapeutics, Inc. - TRDA

  • Independent Safety Data Monitoring Committee Recommends Initiation of Cohort 2 at the Increased Dose of 10 mg/kg in Entrada Therapeutics' ELEVATE-45-201 Study

  • Independent Safety Data Monitoring Committee Recommends Initiation of Cohort 2 at the Increased Dose of 10 mg/kg in Entrada Therapeutics’ ELEVATE-45-201 Study

  • Entrada Therapeutics Announces Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)

  • INVESTOR ALERT: Pomerantz Law Firm Investigates Claims On Behalf of Investors of Entrada Therapeutics, Inc. - TRDA

  • INVESTOR ALERT: Pomerantz Law Firm Investigates Claims On Behalf of Investors of Entrada Therapeutics, Inc. - TRDA

  • INVESTOR ALERT: Pomerantz Law Firm Investigates Claims On Behalf of Investors of Entrada Therapeutics, Inc. - TRDA

  • INVESTOR ALERT: Pomerantz Law Firm Investigates Claims On Behalf of Investors of Entrada Therapeutics, Inc. - TRDA

  • INVESTOR ALERT: Investigation of Entrada Therapeutics, Inc. (TRDA) announced by Holzer & Holzer, LLC

  • TRDA Investors Have Opportunity to Join Entrada Therapeutics, Inc. Fraud Investigation with the Schall Law Firm

  • TRDA Investors Have Opportunity to Join Entrada Therapeutics, Inc. Fraud Investigation with the Schall Law Firm

  • INVESTOR ALERT: Pomerantz Law Firm Investigates Claims On Behalf of Investors of Entrada Therapeutics, Inc. - TRDA

  • Entrada Therapeutics, Inc. (TRDA) Q1 2026 Earnings Call Transcript

  • Entrada Therapeutics, Inc. Shareholders Are Encouraged to Reach Out to Johnson Fistel for More Information About Potentially Recovering Their Losses

  • Entrada Therapeutics DMD Trial Shows Early Functional Gains, Clean Safety Profile

  • Entrada Therapeutics Clinical Trial Data Sparks Brutal Stock Selloff - Here's Why

  • Entrada Therapeutics, Inc. (TRDA) Reports Q1 Loss, Misses Revenue Estimates

  • Entrada Therapeutics Reports First Quarter 2026 Financial Results