Analyst Ratings January 28, 2026

Korro Bio Shares Flat as Jones Trading Keeps Hold Rating; Pipeline Progress and Cash Runway Underlined

KRRO-121 RNA editor advances toward IND filing timeline while mixed clinical results from KRRO-110 weigh on analyst sentiment

By Priya Menon KRRO
Korro Bio Shares Flat as Jones Trading Keeps Hold Rating; Pipeline Progress and Cash Runway Underlined
KRRO

Korro Bio (KRRO) saw Jones Trading reaffirm a Hold rating after the company's Virtual Analyst Day. The stock, trading at $10.74 and up sharply over the past week, is viewed as trading below InvestingPro Fair Value. Management outlined KRRO-121, an RNA editing approach targeting ammonia detoxification via stabilization of Glutamate Synthetase, with IND-enabling work underway and a Phase 1 filing planned for the second half of 2026. The company holds $102.5 million in cash, has reduced its workforce by 34%, and projects a financial runway into the second half of 2027.

Key Points

  • Jones Trading reaffirmed a Hold rating on Korro Bio following the company's Virtual Analyst Day; shares were trading at $10.74 and had risen 13.41% over the past week.
  • KRRO-121 is an RNA editor intended to lower ammonia by stabilizing Glutamate Synthetase; Korro plans IND-enabling work with a Phase 1 filing targeted in H2 2026 and initial data expected in 2027.
  • Korro reported $102.5 million in cash as of Q3 2025 and implemented a 34% workforce reduction, extending the company's runway into H2 2027; InvestingPro data shows rapid cash burn but a current ratio of 6.71.

Korro Bio Inc. (NASDAQ: KRRO) emerged from its Virtual Analyst Day with Jones Trading reiterating a Hold rating on the stock. Shares were trading at $10.74 at the time of reporting and, despite recent volatility, climbed 13.41% over the prior week. InvestingPro Fair Value analysis still flags the stock as potentially undervalued even as investor reaction remains mixed.


Program focus and mechanism

At the center of Korro's presentation was KRRO-121, an RNA editing therapy designed to reduce blood ammonia in patients suffering from Urea Cycle Disorders (UCDs) and Hepatic Encephalopathy (HE). The program aims to introduce a de novo edit that stabilizes Glutamate Synthetase, an enzyme that can clear ammonia independently of the urea cycle - a mechanistic distinction Korro highlighted during the briefing.

The company estimates roughly 4,200 U.S. patients live with severe UCD and that up to 80,000 U.S. patients with HE experience elevated ammonia levels. Preclinical evidence presented by Korro indicates that editing rates in the range of 20-25% of hepatocytes may be sufficient to achieve a therapeutic rescue in disease models.


CTI path and timeline

Korro said it is executing IND-enabling activities for KRRO-121 and intends to file for Phase 1 initiation in the second half of 2026. That timing positions an initial clinical data readout in 2027, assuming regulatory interactions and study start timelines proceed as planned.


Balance sheet and cost actions

On the financial side, Korro reported $102.5 million in cash as of the third quarter of 2025. The company also implemented a 34% workforce reduction, a cost-cutting move management expects will extend the companys cash runway into the second half of 2027. InvestingPro data in the company briefing signaled rapid cash consumption; at the same time, Korro's current ratio stood at 6.71, indicating liquid assets materially exceed its short-term liabilities.


Analyst moves and program setbacks

Analyst coverage has been active following the Virtual Analyst Day. Jones Trading reiterated its Hold rating, citing the potential of the KRRO-121 RNA editor to stabilize Glutamate Synthetase. Clear Street adjusted its coverage by raising its price target to $10 while maintaining a Hold rating after discussing KRRO-121.

Conversely, the company has faced setbacks tied to a different program, KRRO-110. H.C. Wainwright downgraded Korro from Buy to Neutral after KRRO-110 failed to meet expected clinical performance, delivering only an approximately 2 micromolar (~2 M) increase in functional M-AAT - a result the firm said fell short of the therapeutic threshold. William Blair similarly moved its recommendation from Outperform to Market Perform, characterizing the REWRITE study results for KRRO-110 as a material disappointment.


Corporate updates

Management also disclosed an amended employment agreement with Jeffrey Cerio. The revised terms include an increased annual base salary of $425,000 for 2025 and enhanced severance provisions.


Outlook

The confluence of a progressing preclinical-to-clinical transition for KRRO-121, a meaningful cash position supplemented by a workforce reduction, and mixed signals from clinical readouts on KRRO-110 has produced a balanced investor view reflected in reiterated Hold ratings. The company's stated timeline targets a Phase 1 filing in the second half of 2026 and an initial data readout in 2027, while financial measures are intended to preserve operating flexibility into the second half of 2027.

Risks

  • Clinical risk from prior program KRRO-110, which failed to reach expected therapeutic levels (only ~2 M increase in functional M-AAT), has prompted downgrades and underscores the uncertainty inherent in development-stage biotech - impacts healthcare and biotech investment sectors.
  • Execution risk on the KRRO-121 timeline, as IND-enabling activities and a H2 2026 Phase 1 filing target could be affected by regulatory or operational delays - impacting clinical development schedules and investor expectations in biotech.
  • Financial sustainability risk due to ongoing cash burn despite a strong current ratio; while the company expects its cost reductions to extend runway into H2 2027, continued expenditure or unforeseen costs could pressure liquidity - relevant to biotech financing and capital markets.

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