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RNAZ

Transcode Therapeutics, Inc.

Biopharma developer (SEC filing verified)·Phase 3·Boston, MA, United States·CEO: Dr. Philippe P. Calais Ph.D., Pharm., Pharm.D.
Oncology

RNAZ evidence brief

What we can confirm

BioSniper Score:
6.3 / 10
Market Cap:
$1.8M
Lead Asset:
seviprotimut-l (Phase 3)

What it means

The company data is ready for cross-source review; unsupported conclusions remain unknown.

What to watch

Market Cap: $1.8M · Lead Asset: seviprotimut-l (Phase 3)
BioSniper AIPage evidence connected

Prepared research question

What matters most for RNAZ—catalysts, financial risk and supporting evidence?

Run cited research

Traceable citations · Unknowns marked

BioSniper AI · RNAZ

Transcode Therapeutics, Inc. (RNAZ) is a clinical-stage biotechnology company developing RNA-based therapeutics and immuno-oncology programs for advanced and metastatic cancers, with its lead candidate TTX-MC138 in Phase 1/2a trials.

Key risk: Cash runway limited

6.3/10

BioSniper Score

Based on 3 of 6 signals

Limited data coverage

Market Cap

$1.8M

Cash Runway

—

Lead Asset

seviprotimut-l (Phase 3)

Next Catalyst

—

Financial data as of Jun 30, 2026.

Tracking 5 pipeline candidates · 1 clinical trial for Transcode Therapeutics, Inc..

AI OverviewAI overview is shown in English only.

Transcode Therapeutics, Inc. (RNAZ) is a clinical-stage biotechnology company developing RNA-based therapeutics and immuno-oncology programs for advanced and metastatic cancers, with its lead candidate TTX-MC138 in Phase 1/2a trials.

  • Lead candidate TTX-MC138, an antisense inhibitor of microRNA-10b delivered via the proprietary TTX platform, is in Phase 1/2a for advanced solid tumors [pipeline].
  • Phase 1a trial of TTX-MC138 met its primary safety endpoint with positive tolerability and disease stabilization in multiple patients, with no dose-limiting toxicities [news · 2026-06-03].
  • Cash and equivalents were $8.4M as of 2026-06-30, with net income of -$6.8M and shareholders' equity of -$27.7M [sec].
  • The company expects its cash to support operations through approximately year-end 2026, but anticipates needing additional capital for continued R&D and clinical costs [sec_mda · as of 2026-08-14].
  • TransCode has a collaboration with Quantum Leap Health Care Collaborative to evaluate TTX-MC138 in the PRE-I-SPY clinical trial platform [pipeline].

What works

  • Phase 1a trial of TTX-MC138 successfully met its primary safety endpoint with positive tolerability and no dose-limiting toxicities, and showed disease stabilization in multiple patients [news · 2026-06-03].
  • The company's TTX platform is designed for tumor-targeted RNA delivery, potentially enabling previously undruggable RNA targets [sec_mda · as of 2026-04-15].
  • TransCode has a collaboration with Quantum Leap Health Care Collaborative to evaluate TTX-MC138 in the PRE-I-SPY clinical trial platform, which may accelerate development [pipeline].

What to weigh

  • The company has negative shareholders' equity of -$27.7M as of 2026-06-30 and a net loss of -$6.8M, indicating ongoing financial strain [sec].
  • Cash of $8.4M as of 2026-06-30 is expected to fund operations only through approximately year-end 2026, and the company will require additional capital for continued R&D and clinical activities [sec_mda · as of 2026-08-14].
  • TransCode has no product revenue and its ability to achieve profitability depends on successful development and commercialization of product candidates, which is uncertain [sec_mda · as of 2026-08-14].
  • The accumulated deficit is approximately $122.4 million as of 2026-08-14, reflecting substantial historical losses [sec_mda · as of 2026-08-14].

From the filings

Quoted directly from source documents.

  • Phase 1a trial of TTX-MC138 met safety endpoint with disease stabilization

    “The trial met its primary endpoint of safety, with positive tolerability, combined with disease stabilization in multiple patients, and the absence of dose-limiting toxicities with its lead therapeutic candidate TTX-MC138.”

    News · June 3, 2026

  • Cash expected to support operations through year-end 2026

    “We believe that this cash, along with the proceeds from the sale of the Second Convertible Note, will be sufficient to support our operating expenses and capital expenditure requirements through approximately year end 2026.”

    SEC MD&A · August 14, 2026

  • Accumulated deficit of approximately $122.4 million

    “of approximately $122.4 million.”

    SEC MD&A · August 14, 2026

  • TTX-MC138 is an antisense inhibitor of microRNA-10b delivered via TTX platform

    “Antisense inhibitor of oncogenic microRNA-10b”

    Pipeline

Risks & what to watch (4)›

Key risks

  • Cash runway limited — Cash of $8.4M as of 2026-06-30 expected to fund operations only through year-end 2026; additional capital needed [sec_mda · as of 2026-08-14].
  • No product revenue — Company has no product revenue; profitability depends on successful development and commercialization, which is uncertain [sec_mda · as of 2026-08-14].
  • Negative equity and accumulated deficit — Shareholders' equity -$27.7M and accumulated deficit ~$122.4M as of 2026-08-14, indicating significant financial liabilities [sec] [sec_mda · as of 2026-08-14].
  • Clinical development risk — TTX-MC138 is still in early Phase 1/2a; no assurance of regulatory approval or commercial success [pipeline].

What to watch

  • Progress of the ongoing Phase 2a colorectal cancer trial of TTX-MC138 [news · 2026-09-03].
  • Ability to secure additional financing given cash runway ending around year-end 2026 [sec_mda · as of 2026-08-14].
  • Updates from the collaboration with Quantum Leap Health Care Collaborative on the PRE-I-SPY trial platform [pipeline].
  • Further clinical data from the Phase 1a follow-up and any new catalysts discussed in investor webinars [news · 2026-09-28].

Sources: News · Pipeline · SEC MD&A · Generated October 11, 2026 · How we verify sources →

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Evidence & data

Score breakdownBased on 3 of 6 signals · derived from public data

Cash RunwayN/A

Cash runway data unavailable

Financial Health2.0

Net income -$7M

Pipeline Maturity8.5

Lead: Phase 3

Pipeline Breadth8.5

5 candidates

Catalyst MomentumN/A

No upcoming catalysts tracked

Insider SignalN/A

No insider transactions in the last 180 days

Pipeline

Regulatory

Financials

Institutional Holdings

Source: SEC Form 13F · as of Mar 2026

Institutional holders

8

Total value held

$266K

Short Interest

as of Apr 21, 2026
% of float
5.5%
Days to cover
4.9
Shares short
49,976
Daily short volume
-

Short percent of float and days-to-cover reflect reported short positioning. Daily short volume is the exchange-reported short share of a single day's trading volume and is noisier. See the most-shorted biotech ranking →

RNAZ short interest

Governance

Frequently asked questions

What is the AI investment thesis for Transcode Therapeutics, Inc.?

Transcode Therapeutics, Inc. (RNAZ) is a clinical-stage biotechnology company developing RNA-based therapeutics and immuno-oncology programs for advanced and metastatic cancers, with its lead candidate TTX-MC138 in Phase 1/2a trials.

What is Transcode Therapeutics, Inc.'s lead drug candidate?

Transcode Therapeutics, Inc.'s most advanced tracked candidate is seviprotimut-l (Phase 3) for Adjuvant treatment of patients with Stages IIB and IIC melanoma.

Who is the CEO of Transcode Therapeutics, Inc.?

Dr. Philippe P. Calais Ph.D., Pharm., Pharm.D. is the chief executive officer of Transcode Therapeutics, Inc. (RNAZ).

Where is Transcode Therapeutics, Inc. headquartered?

Transcode Therapeutics, Inc. (RNAZ) is headquartered in Boston, MA, United States.

What therapeutic areas does Transcode Therapeutics, Inc. focus on?

Transcode Therapeutics, Inc. develops therapies across Oncology.

923 companies304,840 SEC filings22,637 clinical trials100% citation-verification pass rate (7d)How we verify →

The AI overview and BioSniper Score are neutral, data-derived signals built from public SEC filings, ClinicalTrials.gov and FDA records — not investment advice.