Alentis Therapeutics Revenue and Competitors
Estimated Revenue & Valuation
- Alentis Therapeutics's estimated annual revenue is currently $14.1M per year.
- Alentis Therapeutics's estimated revenue per employee is $201,000
Employee Data
- Alentis Therapeutics has 70 Employees.
- Alentis Therapeutics grew their employee count by 79% last year.
Alentis Therapeutics's People
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Alentis Therapeutics Competitors & AlternativesAdd Company
Competitor Name | Revenue | Number of Employees | Employee Growth | Total Funding | Valuation |
---|---|---|---|---|---|
#1 | $10.5M | 52 | 2% | N/A | N/A |
#2 | $155.6M | 774 | 7% | N/A | N/A |
#3 | $40.8M | 203 | 10% | N/A | N/A |
#4 | $245.6M | 1222 | -24% | N/A | N/A |
#5 | $142.3M | 708 | 0% | N/A | N/A |
#6 | $141.1M | 702 | -9% | N/A | N/A |
#7 | $16.7M | 83 | 28% | N/A | N/A |
#8 | $16.5M | 82 | 8% | N/A | N/A |
#9 | $21.3M | 106 | 15% | N/A | N/A |
#10 | $13.7M | 68 | -1% | N/A | N/A |
What Is Alentis Therapeutics?
Alentis Therapeutics, the Claudin-1 (CLDN1) company, is a clinical stage biotechnology company that focuses on developing first-in-class breakthrough treatments for CLDN1+ tumors and organ fibrosis. \n\nAlentis is pioneering a novel approach to modify and reverse the course of disease progression targeting CLDN1, a previously unexploited target that plays a key role in the pathology of tumors and fibrotic diseases across multiple organs. Alentis is the only company developing potential treatments for solid cancers and fibrosis targeting CLDN1. \n\nAlentis’ portfolio of anti-CLDN1 monoclonal antibodies includes a novel class of anti-cancer therapies designed to reprogram the tumor microenvironment (TME). The interplay between cancer cells and their surrounding microenvironment is highly promising for drug development as many cancers use the TME to build barriers that shield against immune system attacks. Alentis’ lead oncology asset, ALE.C04, is the first potential treatment to target CLDN1 in solid tumors.\n\nIn addition, Alentis’ pipeline includes first-in-class therapies designed to modify and reverse the course of advanced organ fibrosis. ALE.F02, which is currently in Phase 1 clinical trials, is designed to target pathological overexpression of CLDN1 outside of the tight junction to resolve and reverse organ fibrosis and is being investigated for the treatment of fibrotic disease in the kidney, lung, and liver. \n\nThe company was founded in 2019 based on ground-breaking research in the laboratory of Prof. Thomas Baumert MD at the University of Strasbourg and the French National Institute of Health (Inserm). \n\nAlentis is headquartered in Basel’s pharma-biotech hub in Switzerland with a subsidiary for R&D in Strasbourg, France. For more information, please visit us at www.alentis.ch or write to: info@alentis.ch
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Total Funding
70
Number of Employees
$14.1M
Revenue (est)
79%
Employee Growth %
N/A
Valuation
N/A
Accelerator
Company Name | Revenue | Number of Employees | Employee Growth | Total Funding |
---|---|---|---|---|
#1 | $15.5M | 119 | -6% | N/A |
#2 | $115.3M | 375 | 8% | N/A |