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Industries
Biotechnology
Healthcare
Company Size
51-200
Company Stage
Series B
Total Funding
$154.7M
Headquarters
Cambridge, Massachusetts
Founded
2018
Alltrna focuses on developing tRNA therapeutics to treat diseases caused by genetic mutations. Their main product involves engineered tRNAs that can recognize and read stop codons, which are errors in the genetic code that lead to the production of incomplete proteins. By delivering the correct amino acids, these tRNAs help restore the synthesis of full-length proteins, potentially addressing a wide range of diseases linked to nonsense mutations. Unlike other biotech companies, Alltrna is the first to explore the therapeutic potential of tRNA in this way, aiming to unlock new treatment options for patients with specific genetic disorders. The goal of Alltrna is to provide effective therapies that target the root causes of diseases, improving the quality of life for those affected.
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Total Funding
$154.7M
Above
Industry Average
Funded Over
2 Rounds
Industry standards
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Unlimited Paid Time Off
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Professional Development Budget
CAMBRIDGE, Mass., Jan. 6, 2025 /PRNewswire/ -- Alltrna , a Flagship Pioneering company unlocking transfer RNA (tRNA) biology and pioneering tRNA therapeutics to regulate the protein universe and resolve disease, today announced the appointment of Dr. Nerissa Kreher as Chief Medical Officer (CMO). Dr. Kreher brings decades of expertise in rare disease drug development, including extensive experience in clinical development, medical affairs, and regulatory strategy across both early- and late-stage programs."We are thrilled to welcome Nerissa to the Alltrna leadership team as we advance our first tRNA development candidates to the clinic for liver Stop Codon Disease," said Michelle C. Werner, CEO of Alltrna
CAMBRIDGE, Mass., April 22, 2024 /PRNewswire/ -- Alltrna , a Flagship Pioneering company unlocking transfer RNA (tRNA) biology and pioneering tRNA therapeutics to regulate the protein universe and resolve disease, today announced a poster presentation at the American Society of Gene & Cell Therapy (ASGCT) 27th Annual Meeting taking place May 7-11 in Baltimore and a talk and two poster presentations at TIDES USA 2024 taking place May 14-17 digitally and in-person in Boston.Details of the presentations are as follows:ASGCT 27th Annual MeetingPoster Title: tRNA Therapeutics to Treat Stop Codon DiseaseSession Date & Time: May 9, 12:00 PM to 7:00 PM ETPresenter: Stephen Eichhorn, Ph.D., Head of Computational and Molecular Biology, AlltrnaPresentation Room: Exhibit HallSession Title: Oligonucleotide TherapeuticsAbstract Number: 1221TIDES USA 2024Talk Title: Manufacturing Strategies for Chemically Modified tRNAsSession Date & Time: May 17, 5:00 PM to 5:30 PM ETPresenter: William Kiesman, Ph.D., Chief Technology Officer, AlltrnaSession Title: Oligonucleotide Chemistry, Manufacturing, and ControlsPoster Title: Building 3-D homology models to support tRNA structure-based drug designPresenter: Audrey Hughes, Ph.D., Scientist II, Computational Chemistry, AlltrnaPoster Title: Quantification of Tissue Delivery for tRNA Therapeutics in LNP FormulationsPresenter: W. George Lai, Ph.D., Head of DMPK, Drug Safety and Clinical Pharmacology, AlltrnaPosters will be displayed onsite in the exhibit hall throughout TIDES USA 2024.About Stop Codon DiseaseStop Codon Disease encompasses thousands of rare and common diseases that stem from premature termination codons (PTC) also called nonsense mutations, where the code for an amino acid has been mutated into a premature "stop" codon. This results in a truncated or shortened protein product with no or altered biological activity that causes disease. Approximately 10% of all people with a genetic disease have Stop Codon Disease, representing approximately 30 million people worldwide. Alltrna is engineering tRNA medicines that can read these PTC mutations and deliver the desired amino acid, thereby restoring the production of the full-length protein.About AlltrnaAlltrna unlocks tRNA biology to treat disease. The company's platform incorporates AI/ML tools to develop and deliver diverse programmable molecules with broad therapeutic potential
Alltrna Announces Series B Raise of $109M Back to HomeCAMBRIDGE, MA, Alltrna, a company unlocking transfer RNA (tRNA) biology and pioneering tRNA medicines, has raised $109 million in a Series B financing.Alltrna, a Flagship Pioneering company unlocking transfer RNA (tRNA) biology and pioneering tRNA medicines to regulate the protein universe and resolve disease, announced that it has raised $109 million in a Series B financing to advance the company's platform and first drug candidates towards the clinic for a first indication in Stop Codon Disease. The financing round included the company's founder, Flagship Pioneering, and a number of top-tier investors.(c)2011-2020 by Massinvestor, Inc. For contact info, please check out our about page
Alltrna, a Flagship Pioneering company unlocking transfer RNA (tRNA) biology and pioneering tRNA therapeutics to regulate the protein universe and resolve disease, today announced that it has appointed Chris Henderson, Ph.D., as Chief Scientific Officer and promoted William (Will) Kiesman, Ph.D., to Chief Technology Officer.
Alltrna is working on novel science around transfer RNA (tRNA), with the goal of creating a new class of medicines to regulate proteins.
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Industries
Biotechnology
Healthcare
Company Size
51-200
Company Stage
Series B
Total Funding
$154.7M
Headquarters
Cambridge, Massachusetts
Founded
2018
Find jobs on Simplify and start your career today