Fundraising Fox

Syrna Therapeutics

Del Mar, US · Founded 2020 · Delaware corporation · 2 known investors

Syrna Therapeutics is a biotech company developing small-molecule covalent translation inhibitors that bind and modify structured domains in the mRNA of disease-causing proteins to block their expression. It uses a 3D structure-guided drug discovery platform, with lead programs in immunology and neurodegeneration and a broader pipeline spanning metabolic disease and oncology.

Also known as Syrna · Syrna Therapeutics, Inc.

Founders & leadership

THThomas Hermann
Thomas HermanninCo-Founder, Scientific Advisor & Board Director
AA
Aiden AcevesNamed on SEC filing
DWDavid Weitz
David WeitzinCEO/Founder

Board

JDJoel Dudley
Joel Dudleyin𝕏Board directorVenture Partner at Innovation Endeavors

Investors · 2

Reported raises · per SEC filings

Form D private placements

$10.9M disclosed across 1 round · 2023

$10.9MraisedAug 2023 · 3 investors · Biotechnology
Rule 506(b)
Officers, directors & promoters on the filing
  • Thomas HermannDirector
  • Aiden AcevesDirector
  • Joel DudleyDirector
  • David WeitzExecutive Officer, Director
Offering amount
$10.9M
Amount sold
$10.9M
First sale
Aug 2023
Incorporated
Corporation, Delaware, 2020
Federal exemptions
06b
Full filing on SEC EDGAR ↗

Source: SEC EDGAR Form D. Amounts as filed; amended filings shown once at their latest values.

Company profile

researched Aug 2026

Syrna Therapeutics, Inc. is a biotechnology company working on small-molecule drugs that silence disease-causing proteins by covalently modifying their messenger RNA. Its inhibitors bind unique sites within structured domains of a target mRNA and chemically modify them, obstructing the ribosome and preventing translation of the encoded protein. The company states that this mechanism is independent of the underlying biology of the site being modified, so it can in principle be applied to any mRNA containing a druggable structured domain.

The company's discovery engine is a 3D structure-informed platform that identifies structured domains in the mRNA of disease-causing proteins and validates them as small-molecule target sites. Syrna characterizes these domains as large, stable, persistent and complex, with sequence and structural features that support selective, high-affinity binding. It reports routinely identifying druggable structured domains in human mRNA and having found such domains in the mRNA of more than 25 disease-causing proteins spanning diverse protein classes.

Syrna's disclosed portfolio comprises programs in early lead optimization against immunology and neurodegeneration targets, supported by a broader asset base of druggable structured mRNA domains in immunology, neurodegeneration, metabolic disease and oncology, several of which are accompanied by chemistry assets.

Founding story

Syrna was founded on the premise that halting production of disease-causing proteins by interfering with cellular translation requires a fundamentally new approach, pairing 3D structure-guided discovery for mRNA with a universal translation-inhibition mechanism. Co-founders include David Weitz, President and CEO, and Thomas Hermann, acting CTO.

Business model

Syrna is a therapeutics developer advancing an internal pipeline of small-molecule mRNA-targeting programs and states that it welcomes partnering opportunities to accelerate its portfolio.

Traction

Programs targeting immunology and neurodegeneration mRNAs are in early lead optimization, and the company reports identifying druggable structured domains in the mRNA of more than 25 disease-causing proteins, with chemistry assets attached to many of the broader portfolio targets.

Latest developments

The company emerged from stealth with its covalent translation inhibitor platform, and on January 7, 2026 was featured on the Innovating Tomorrow's Medicine interview series, where CEO David Weitz discussed targeting mRNA with small molecules.

Full profile — market position, technology, go-to-market, geography

Market position

Syrna describes itself as the first mRNA-focused structure-guided drug discovery company, noting that structure-guided methods, while established for protein targets, have been absent from small-molecule programs aimed at mRNA.

Technology

Syrna applies structure-guided drug discovery — an approach historically used for protein targets — to mRNA, making 3D structures of mRNA accessible for both target identification and medicinal chemistry. Resolving the three-dimensional structure of drug-binding sites in mRNA informs where and how small molecules bind, which the company uses to design covalent inhibitors that modify the RNA and block ribosomal translation of the target transcript.

Go-to-market

The company advances proprietary programs from target identification through lead optimization and seeks partnerships to accelerate portfolio development.

Prospective partners and licensees in the pharmaceutical industry, with therapeutic programs directed at immunology, neurodegeneration, metabolic disease and oncology indications.

Geography

Syrna Therapeutics is headquartered at 10835 Road to the Cure, Suite 150, San Diego, California 92121.

Compiled by commissioned research from 1 cited public sources — announcements, filings, and press listed under research sources below.

Key figures

latest reported
Disease-causing proteins with identified druggable structured mRNA domainsJan 202525 targets

Company-reported or press-reported figures, each dated to when it was claimed — not independently audited.

Founder mafia

2 people who came through Syrna Therapeutics went on to found or lead other companies.

Competitors · 7

by search overlap
Sionnatx30 shared keywordsSionna Therapeutics is a biopharmaceutical company founded in 2019 that develops small-molecule therapies for cystic fibrosis by targeting and stabilizing NBD1, the domain of the CFTR protein where the common ΔF508 mutation occurs. It is advancing a portfolio of NBD1 stabilizers and complementary CFTR modulators intended to be used in combination to normalize CFTR function in CF patients.
Sirnaomics28 shared keywordsSirnaomics is an RNA therapeutics company developing RNA interference (RNAi) drugs using its proprietary PNP (Peptide Nanoparticle) delivery platform for extra-hepatic delivery and its GalAHead technology for controlling therapeutic duration. Its pipeline spans oncology, regenerative and aesthetic medicine, and cardiovascular and metabolic diseases.
Ronatherapeutics27 shared keywordsRona Therapeutics develops siRNA-based therapeutics using its GAIA platform to target metabolic and cardiovascular conditions including hypertriglyceridemia, obesity, ASCVD, and MASH. Its pipeline includes APOC3, INHBE, PCSK9-Lp(a), and angiotensinogen-targeting candidates for patients with cardiovascular and metabolic diseases.
Switch Therapeutics26 shared keywordsSwitch Therapeutics develops RNA interference (RNAi) therapeutic applications targeting central nervous system diseases, leveraging research from Caltech, Harvard Medical School, and City of Hope.
Serna Bio23 shared keywordsSerna builds a platform to unlock the transcriptome as a drug target for drug discovery. The company integrates technology and biology to change drug discovery processes.
Siriusrna22 shared keywordsSirius Therapeutics is a biopharmaceutical company developing siRNA-based therapeutics, including work in the anti-coagulant therapeutic area. It focuses on drug discovery and clinical development of RNA-based medicines.
Bioworld16 shared keywordsBioWorld is a suite of daily news and data services covering therapeutics, medical technology, biopharma business transactions, and drug R&D, serving biopharmaceutical and medtech industry professionals. Owned by Clarivate, it publishes products including BioWorld, BioWorld Science, and BioWorld Asia with reporting from writers stationed globally.

Companies competing with Syrna Therapeutics for the same Google search keywords, organic and paid, via search-intersection analysis.

Timeline · 2

launches, deals, and filings
Jan 2026
Syrna featured on Innovating Tomorrow's Medicine interview series

CEO David Weitz appeared in a video interview, 'Targeting mRNA with Small Molecules,' on the Innovating Tomorrow's Medicine series covering healthcare, biotechnology and life sciences.

source ↗

Jan 2025
Syrna Therapeutics emerges from stealth

The company announced it was coming out of stealth with a covalent translation inhibitor approach targeting mRNA, built on 3D structure-guided drug discovery.

source ↗

Dated company events from announcements, filings, and press; legal rows summarize public dockets and regulator releases.

Legal entities · 1

corporate structure
Syrna TherapeuticsDelaware

In the news

Research sources · 1

primary sources listed

1 public sources were cited for this profile; the first-party ones are listed here.

Frequently asked questions

What does Syrna Therapeutics do?
Syrna Therapeutics develops small-molecule covalent translation inhibitors that block protein expression by modifying mRNA.
Who are Syrna Therapeutics's investors?
Syrna Therapeutics's investors include Innovation Endeavors, Insight Partners.
How much funding has Syrna Therapeutics raised?
Syrna Therapeutics has disclosed $10.9M raised across 1 round.
Where is Syrna Therapeutics headquartered?
Syrna Therapeutics is headquartered in Del Mar, US.