Skip to main content
KRRONasdaq

Korro Bio, Inc.

Biopharma developer (SEC filing verified)·Phase 1·Cambridge, MA, United States·CEO: Dr. Ram Aiyar MBA, Ph.D.
Neurology

KRRO evidence brief

What we can confirm

No verified snapshot fields are available yet.

What it means

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

What to watch

Watch the next source-backed data update.
BioSniper AIPage evidence connected

Prepared research question

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

Run cited research

Traceable citations · Unknowns marked

BioSniper AI · KRRO

Korro Bio, Inc. is a biopharmaceutical company developing RNA editing oligonucleotide therapies for rare and prevalent diseases, with lead programs targeting Alpha-1 Antitrypsin Deficiency and Urea Cycle Disorders.

Key risk: No approved products or revenue

5.3/10

BioSniper Score

Based on 6 of 6 signals

Market Cap

$190.1M

Cash Runway

19.8 mo

Lead Asset

aatd program (Preclinical)

Financial data as of Jun 30, 2026.

Tracking 5 pipeline candidates · 2 clinical trials · 1 catalyst for Korro Bio, Inc..

Similar companies

AI OverviewAI overview is shown in English only.

Korro Bio, Inc. is a biopharmaceutical company developing RNA editing oligonucleotide therapies for rare and prevalent diseases, with lead programs targeting Alpha-1 Antitrypsin Deficiency and Urea Cycle Disorders.

  • Korro Bio is developing a new class of genetic medicines based on RNA editing, using an oligonucleotide approach to achieve a precise adenosine-to-inosine change [sec · filed 2026-03-13].
  • The company has two lead programs: KRRO-110 for Alpha-1 Antitrypsin Deficiency (AATD) and KRRO-121 for Urea Cycle Disorders (UCDs) [sec · filed 2024-11-21][sec · filed 2026-08-19].
  • KRRO-121 received ethics committee submission in Australia to initiate a first-in-human Phase 1/2 clinical trial for UCDs [sec · filed 2026-08-19].
  • As of June 30, 2026, Korro Bio reported cash and equivalents of $24.9M, zero revenue, and a net loss of $18.9M [sec].
  • The company has a research collaboration and license agreement with Novo Nordisk [sec · filed 2025-11-12].

What works

  • Korro Bio's RNA editing platform offers a differentiated approach that may provide increased specificity and tunability compared to DNA editing, potentially expanding the reach of genetic medicines [sec · filed 2026-03-13].
  • The company has advanced two programs into clinical development (KRRO-110 for AATD and KRRO-121 for UCDs), demonstrating platform progress [sec · filed 2024-11-21][sec · filed 2026-08-19].
  • A research collaboration with Novo Nordisk provides external validation and potential resources for development [sec · filed 2025-11-12].

What to weigh

  • Korro Bio has no approved products and has generated zero revenue as of June 30, 2026, with a net loss of $18.9M in the latest quarter [sec].
  • The company's cash position of $24.9M as of June 30, 2026, may be limited to fund ongoing clinical trials and operations without additional financing [sec].
  • Clinical development risks are inherent, including potential delays, regulatory hurdles, and competition from other RNA-targeting therapies [sec · filed 2026-03-09].

From the filings

Quoted directly from source documents.

  • Korro Bio is developing RNA editing therapies using an oligonucleotide approach.

    We are a biopharmaceutical company with a mission to discover, develop and commercialize a new class of genetic medicines based on editing RNA, enabling the treatment of both rare and highly prevalent diseases.

    SEC filings · March 13, 2026

  • Korro Bio has a collaboration with Novo Nordisk.

    status of the research collaboration and license agreement with Novo Nordisk

    SEC filings · November 12, 2025

Catalyst timeline

  • 2026-09-01 · Phase 2 Start: A Phase 1/2, Randomized, Double-Blind, Placebo-Controlled, Single- and Multiple-Ascending Dose StudyThe company is expected to initiate a Phase 1/2 clinical trial for KRRO-121 in Urea Cycle Disorders, with the trial design including randomized, double-blind, placebo-controlled, single- and multiple-ascending dose cohorts.
Risks & what to watch (4)

Key risks

  • No approved products or revenueKorro Bio has no marketed products and reported zero revenue as of June 30, 2026, with a net loss of $18.9M [sec].
  • Limited cash runwayCash and equivalents of $24.9M as of June 30, 2026, may be insufficient to fund all planned development without additional capital [sec].
  • Clinical and regulatory risksPre-clinical and clinical studies are subject to delays, failures, and regulatory uncertainties common in biopharmaceutical development [sec · filed 2026-03-09].
  • Dependence on platform technologyThe RNA editing platform is novel and unproven in late-stage trials, with no guarantee of successful translation to approved therapies [sec · filed 2026-03-13].

What to watch

  • Initiation of the Phase 1/2 clinical trial for KRRO-121 in Urea Cycle Disorders, following ethics committee submission in Australia [sec · filed 2026-08-19].
  • Progress of KRRO-110 for Alpha-1 Antitrypsin Deficiency, which received clinical trial approval in Australia in November 2024 [sec · filed 2024-11-21].
  • Future financing events given the limited cash position of $24.9M as of June 30, 2026 [sec].
  • Updates on the Novo Nordisk collaboration and any potential pipeline expansion [sec · filed 2025-11-12].

Sources: Catalysts · Competitor trials · News · SEC filings · Generated August 27, 2026 · How we verify sources →

Run Korro Bio, Inc. through your own thesis

Use the pipeline, catalyst, financial, FDA, and market facts on this page as inputs to a protocol you control.

Your protocol can:

  • Turn available Korro Bio, Inc. facts into screen rules or deeper checks
  • Show cited findings, blockers, and unresolved evidence together
  • Save the logic and rerun it as the company evidence changes
Run a thesis on this company — freeRun a thesis on this company

Evidence & data

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

Cash Runway5.5

19.8 months

Financial Health1.5

OCF -$17M · Net income -$19M

Pipeline Maturity6.0

Lead: Phase 1/Phase 2

Pipeline Breadth8.5

5 candidates

Catalyst Momentum4.0

1 upcoming, next in ~2d

Insider Signal6.2

12 buys · 24 sells (180d)

Runway

Catalysts

Pipeline

Regulatory

Financials

Institutional Holdings

Source: SEC Form 13F · as of Mar 2026

Institutional holders

95

Total value held

$106.6M

Showing top 10 of 95 institutional holders of Korro Bio, Inc.. Open the full 13F history after sign-in.

Short Interest

as of May 21, 2026
% of float
8.7%
Days to cover
7.3
Shares short
1,117,429
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 →

KRRO short interest

Governance

Frequently asked questions

What is the AI investment thesis for Korro Bio, Inc.?

Korro Bio, Inc. is a biopharmaceutical company developing RNA editing oligonucleotide therapies for rare and prevalent diseases, with lead programs targeting Alpha-1 Antitrypsin Deficiency and Urea Cycle Disorders.

What is Korro Bio, Inc.'s lead drug candidate?

Korro Bio, Inc.'s most advanced tracked candidate is aatd program (Preclinical) for Alpha-1 antitrypsin deficiency (AATD).

What is Korro Bio, Inc.'s next catalyst?

Korro Bio, Inc.'s next tracked catalyst is a Phase2_Start event — "Phase 2 Start: A Phase 1/2, Randomized, Double-Blind, Placebo-Controlled, Single- and Multiple-Ascending Dose Study" — expected September 1, 2026.

Who is the CEO of Korro Bio, Inc.?

Dr. Ram Aiyar MBA, Ph.D. is the chief executive officer of Korro Bio, Inc. (KRRO).

Where is Korro Bio, Inc. headquartered?

Korro Bio, Inc. (KRRO) is headquartered in Cambridge, MA, United States.

925 companies232,681 SEC filings21,419 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.