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Prime Medicine Reports First Quarter 2026 Financial Results and Provides Business Updates

(Positive)
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Prime Medicine (Nasdaq: PRME) reported Q1 2026 results and program updates on May 7, 2026. Key points: cash and investments $149.2M as of March 31, 2026, providing a runway into 2027; net loss $49.1M for Q1; R&D $34.1M and G&A $17.4M. The company is on track to file IND/CTA for PM577 (Wilson Disease) H1 2026 and PM647 (AATD) mid-2026, with initial clinical data expected in 2027, and continues regulatory dialogue toward a potential BLA for PM359 (CGD).

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Positive

  • On track to file IND/CTA for PM577 in H1 2026
  • On track to file IND/CTA for PM647 in mid-2026
  • Initial clinical data for PM577 and PM647 expected in 2027
  • $149.2M cash, cash equivalents, investments, and restricted cash as of March 31, 2026
  • Appointed Svetlana Makhni as Chief Financial Officer

Negative

  • Cash balance declined from $191.4M (Dec 31, 2025) to $149.2M
  • Net loss of $49.1M for Q1 2026
  • G&A expenses rose to $17.4M, driven by arbitration-related legal expenses

News Market Reaction – PRME

-8.65%
22 alerts
-8.65% Session close to close
+8.0% Peak Tracked
-2.2% Trough Tracked
$612.43M Market Cap
1.1x Rel. Volume

In the May 7 session, PRME declined 8.65%, reflecting a notable negative market reaction. Argus tracked a peak move of +8.0% during that session. Argus tracked a trough of -2.2% from its starting point during tracking. Our momentum scanner triggered 22 alerts that day, indicating elevated trading interest and price volatility.

Data tracked by StockTitan Argus on the day of publication.

Market Context

The stock moved -8.7% in the session following this news. A negative reaction despite operational pr...
Analysis

The stock moved -8.7% in the session following this news. A negative reaction despite operational progress would fit the historical pattern: earnings and updates previously averaged a -8.71% next-day move. The market may continue to focus on a quarterly net loss of $49.1M and cash of $149.2M, weighing ongoing burn against timelines that extend to initial data in 2027. Such sensitivity has often overshadowed pipeline and leadership advancements.

Key Figures

R&D expenses: $34.1M R&D expenses prior-year: $40.6M G&A expenses: $17.4M +5 more
8 metrics
R&D expenses $34.1M Three months ended March 31, 2026
R&D expenses prior-year $40.6M Three months ended March 31, 2025
G&A expenses $17.4M Three months ended March 31, 2026
G&A expenses prior-year $13.3M Three months ended March 31, 2025
Net loss $49.1M Three months ended March 31, 2026
Net loss prior-year $51.9M Three months ended March 31, 2025
Cash and investments $149.2M As of March 31, 2026
Cash guidance Into 2027 Expected cash runway based on current operating plans

Previous Earnings Reports

5 past events · Latest: Mar 03 (Positive)
Same Type Pattern 5 events
Date Event Sentiment 24h Move Catalyst
Mar 03 Full-year 2025 earnings Positive -9.2% Full-year 2025 results, $191.4M cash and continued CGD and liver program progress.
Nov 07 Q3 2025 earnings Positive -8.8% Q3 2025 results, WD/AATD timelines, $227.0M cash and leadership strengthening.
Nov 07 Q3 2025 earnings Positive -8.8% Q3 2025 update on PM647 and PM577 timelines with cash to fund into 2027.
Aug 07 Q2 2025 earnings Positive -9.6% Q2 2025 loss, first CGD proof-of-concept data and $144.2M follow-on raise.
May 08 Q1 2025 earnings Positive -7.0% Q1 2025 loss widening, $158.3M cash and early WD/AATD pipeline timelines.

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Pattern Detected

Earnings and business update releases have repeatedly coincided with negative next-day moves despite highlighting cash runway and pipeline progress.

Recent Company History

Over the past year, Prime Medicine’s earnings and business updates have focused on advancing PM577 and PM647 toward IND/CTA filings and maintaining cash runway into 2027. Releases on Aug 7, 2025, Nov 7, 2025, and Mar 3, 2026 detailed substantial R&D investment, growing net losses and sizeable cash balances (up to $259.6M). Yet each event saw shares decline around the announcement, indicating a pattern of weak market reception to otherwise progress-oriented updates.

Key Terms

clinical trial application, cta, biologics license application, phase 1/2, +2 more
6 terms
clinical trial application regulatory
"Investigational New Drug application (IND) and/or Clinical Trial Application (CTA) for PM577"
An application submitted to a regulatory authority requesting formal permission to begin testing a new drug, medical device, or treatment in humans. Like asking for a building permit before construction, it summarizes safety data, plans for how the study will be run, and monitoring procedures; investors watch these filings closely because approval lets a program move from lab research to clinical testing, reducing uncertainty and creating value-driving milestones.
cta regulatory
"Investigational New Drug application (IND) and/or Clinical Trial Application (CTA) for PM577"
A CTA (Commodity Trading Advisor) is a professional or firm that manages and advises clients on trading futures, options and other derivatives, similar to a coach who designs and runs strategies using these instruments. It matters to investors because CTAs make decisions that can affect portfolio risk and returns, and they operate under regulatory oversight, so knowing a CTA’s strategy, performance and compliance helps assess potential reward and risk.
biologics license application regulatory
"toward a potential Biologics License Application (BLA) filing for PM359"
A biologics license application is a formal request submitted to regulatory authorities seeking approval to market a new biological medicine, such as vaccines or treatments made from living organisms. It is a comprehensive review process that evaluates the safety, effectiveness, and manufacturing quality of the product. For investors, receiving approval signals that a biological therapy can be sold to the public, potentially leading to revenue growth and market success.
phase 1/2 medical
"from the first two patients treated in its Phase 1/2 study of PM359"
Phase 1/2 is a combined early-stage clinical trial that first tests a new drug or treatment for safety and the right dose, then quickly expands to check if it shows any signs of working in patients. For investors, results from a Phase 1/2 study offer an early read on both risk and potential reward—like a prototype test that both confirms a product won’t harm users and suggests whether it could sell—helping guide valuation and development decisions.
car-t medical
"develop Prime Edited CAR-T products for hematology, immunology and oncology in partnership"
CAR-T is a type of cancer therapy that reprograms a patient’s own immune cells to seek and destroy specific cancer cells, like teaching guard dogs a new scent to track intruders. It matters to investors because CAR-T treatments can command high prices, drive strong revenue for successful developers, and carry regulatory and manufacturing risks that can sharply affect a company’s valuation and long-term growth prospects.
prime editing technical
"designed to deliver on the transformative potential of Prime Editing"
Prime editing is a gene‑editing method that can precisely rewrite small stretches of DNA inside living cells without cutting both strands, functioning like a targeted “find-and-replace” for genetic code rather than tearing out a paragraph. It matters to investors because it expands the range of treatable genetic conditions and may reduce side effects and development risk, influencing biotech valuations, clinical prospects, intellectual property stakes and regulatory outlooks.

AI-generated analysis. How Rhea-AI works. Not financial advice.

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-- On track to file IND and/or CTA for PM577 in Wilson Disease in H1 2026 and for PM647 in AATD mid-2026; initial clinical data from both programs expected in 2027 --
 
-- Continued regulatory dialogue with the FDA toward BLA filing for PM359 in CGD --
 
-- Strengthened leadership team with appointment of Svetlana Makhni as Chief Financial Officer --
 
-- Cash, cash equivalents, investments, and restricted cash of $149.2 million as of March 31, 2026, providing cash runway into 2027 --
 

CAMBRIDGE, Mass., May 07, 2026 (GLOBE NEWSWIRE) -- Prime Medicine, Inc. (Nasdaq: PRME), a biotechnology company committed to delivering a new class of differentiated one-time curative genetic therapies, today reported financial results for the quarter ended March 31, 2026 and provided a business update.

“Prime Medicine continues to execute with clear momentum and a focused strategy designed to deliver on the transformative potential of Prime Editing,” said Allan Reine, M.D., Chief Executive Officer of Prime Medicine. “We remain on track to file regulatory applications for PM577 in Wilson Disease in the first half of this year, and for PM647 in AATD mid-year, bringing two of our most advanced programs to the brink of clinical entry, with initial data from both expected in 2027. In parallel, we continue to progress toward a potential BLA filing for PM359, which, if successful, would bring a one-time, potentially curative therapy to people living with CGD, who today face a lifetime of debilitating infections and limited treatment options. With a strengthened leadership team and a continued commitment to disciplined capital allocation, we believe Prime Medicine is well positioned to execute across our pipeline and unlock the broad promise of Prime Editing for patients.”

Prime Medicine’s Pipeline:

Prime Medicine is currently advancing in vivo programs to cure two of the largest genetic liver diseases, Wilson Disease (WD) and Alpha-1 Antitrypsin Deficiency (AATD). Prime Medicine expects to file an Investigational New Drug application (IND) and/or Clinical Trial Application (CTA) for PM577 in WD in the first half of 2026 and for PM647 in AATD in mid-2026; initial clinical data from both programs are expected in 2027.

Prime Medicine is also advancing an in vivo Cystic Fibrosis (CF) program with support from the Cystic Fibrosis Foundation, and efforts to develop Prime Edited CAR-T products for hematology, immunology and oncology in partnership with Bristol Myers Squibb. Additionally, following positive proof-of-concept data from the first two patients treated in its Phase 1/2 study of PM359 for the treatment of Chronic Granulomatous Disease (CGD), Prime Medicine continues to engage in regulatory dialogue with the U.S. Food and Drug Administration (FDA) toward a potential Biologics License Application (BLA) filing for PM359.

Recent Corporate Updates:

In April 2026, Prime Medicine announced the appointment of Svetlana Makhni as Chief Financial Officer (CFO). Ms. Makhni brings over 20 years of experience across biotechnology and healthcare CFO and investment banking roles, and will oversee Prime Medicine’s financial operations and strategy, including investor relations, and financial planning and analysis.

Upcoming Presentation:

Today, Prime Medicine announced that it will present new preclinical data for its Wilson Disease program at the American Society of Gene & Cell Therapy (ASGCT) 2026 Annual Meeting (May 11-15 in Boston, MA). Details of the oral presentation are as follows:

  • Session: Translational Gene Therapy and Editing in Storage Disorders
  • Presentation ID: 78
  • Presentation Title: Prime Editing Enables Precise and Efficient Correction of ATP7B Mutations and Restoration of Copper Homeostasis in Wilson Disease Models
  • Presentation Date and Time: May 12th, 2026 at 11:30AM EST

First Quarter 2026 Financial Results

  • Research and Development (R&D) Expenses: R&D expenses were $34.1 million for the three months ended March 31, 2026, as compared to $40.6 million for the three months ended March 31, 2025. The decrease in R&D expenses was driven primarily by Prime Medicine’s strategic focus on advancing its in vivo liver franchise, deprioritization of its CGD program, and a reduction in R&D personnel resulting from the workforce reduction. This decrease was partially offset by an increase in clinical expense as Prime Medicine advances its WD and AATD programs.
  • General and Administrative (G&A) Expenses: G&A expenses were $17.4 million for the three months ended March 31, 2026, as compared to $13.3 million for the three months ended March 31, 2025. The increase in G&A expenses was primarily driven by arbitration-related legal expenses, offset by a decrease in personnel costs resulting from the workforce reduction announced in May 2025.
  • Net Loss: Net loss was $49.1 million for the three months ended March 31, 2026, as compared to $51.9 million for the three months ended March 31, 2025.
  • Cash Position: As of March 31, 2026, cash, cash equivalents, investments, and restricted cash were $149.2 million, as compared to $191.4 million as of December 31, 2025.

Financial Guidance

Based on its current operating plans, Prime Medicine expects that its cash, cash equivalents and investments as of March 31, 2026 will be sufficient to fund its operating expenses and capital expenditure requirements into 2027.

About Prime Medicine

Prime Medicine is a leading biotechnology company dedicated to creating and delivering the next generation of gene editing therapies to patients. The Company is deploying its proprietary Prime Editing platform, a versatile, precise and efficient gene editing technology, to develop a new class of differentiated one-time curative genetic therapies. Designed to make only the right edit at the right position within a gene while minimizing unwanted DNA modifications, Prime Editors have the potential to repair almost all types of genetic mutations and work in many different tissues, organs and cell types. Taken together, Prime Editing’s versatile gene editing capabilities could unlock opportunities across thousands of potential indications.

Prime Medicine is currently progressing a diversified portfolio of investigational therapeutic programs organized around our core areas of focus: liver, lung, and immunology and oncology. Across each core area, Prime Medicine is focused initially on a set of high value programs, each targeting a disease with well-understood biology and a clearly defined clinical development and regulatory path, and each expected to provide the foundation for expansion into additional opportunities. Over time, the Company intends to maximize Prime Editing’s broad and versatile therapeutic potential, as well as the modularity of the Prime Editing platform, to rapidly and efficiently expand beyond the diseases in its current pipeline, potentially including additional genetic diseases, immunological diseases, cancers, infectious diseases, and targeting genetic risk factors in common diseases, which collectively impact millions of people. For more information, please visit www.primemedicine.com.

From time to time Prime Medicine may use its website, its X, formerly Twitter, account (@PrimeMedicine) or its LinkedIn profile at https://www.linkedin.com/company/prime-medicine to distribute material information. Its financial and other material information is routinely posted to and accessible on the Investors section of its website, available at www.primemedicine.com. Investors are encouraged to review the Investors section of its website because the Company may post material information on that site that is not otherwise disseminated by the Company. Information that is contained in and can be accessed through the Company’s website or its social media is not incorporated into, and does not form a part of, this press release.

© 2026 Prime Medicine, Inc. All rights reserved. PRIME MEDICINE, the Prime Medicine logos, and PASSIGE are trademarks of Prime Medicine, Inc. All other trademarks referred to herein are the property of their respective owners.

Forward Looking Statements

This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, as amended, including, without limitation, implied and express statements about Prime Medicine’s beliefs and expectations regarding: the significance of data from its Phase 1/2 trial of PM359; the ongoing regulatory interactions with the FDA based on the data from its Phase 1/2 trial of PM359 and the outcomes of any such interactions, including its plan to submit a BLA for PM359 following final alignment with the FDA; the continued development and advancement of its WD, AATD and CF programs, including the anticipated timing of filing an IND and/or CTA application for its WD program in the first half of 2026 and for its AATD program in mid-2026, and initial clinical data for both programs in 2027; the potential of PM359 to address the unmet medical need for patients with CGD; the potential of Prime Editing to correct the causative mutations of, and to cure, diseases, including WD, AATD, CF and CGD; the partnership with Bristol Myers Squibb and the Cystic Fibrosis Foundation and the intended and potential benefits thereof; its expectations regarding the breadth of Prime Editing technology and the implementation of its strategic plans for its business, programs, and technology; the modularity of the Prime Editing platform and the benefits thereof; the potential impacts of Ms. Makhni’s appointment as CFO of the Company; the potential of Prime Editing to unlock opportunities across thousands of potential indications; and its expected cash runway.

Any forward-looking statements in this press release are based on management’s current expectations and beliefs and are subject to a number of risks, uncertainties and important factors that may cause actual events or results to differ materially from those expressed or implied by any forward-looking statements contained in this press release, including, without limitation, risks associated with: uncertainties related to Prime Medicine’s product candidates entering clinical trials; the authorization, initiation, and conduct of preclinical and IND-enabling studies and other development requirements for potential product candidates, including uncertainties related to opening INDs and obtaining regulatory approvals; risks related to the development and optimization of new technologies, the results of preclinical studies, or clinical studies not being predictive of future results in connection with future studies; the scope of protection Prime Medicine is able to establish and maintain for intellectual property rights covering its Prime Editing technology; Prime Medicine’s ability to identify and enter into future license agreements and collaborations; Prime Medicine’s expectations regarding the anticipated timeline of its cash runway and future financial performance; and general economic, industry and market conditions. These and other risks and uncertainties are described in greater detail in the section entitled “Risk Factors” in Prime Medicine’s most recent Annual Report on Form 10-K, as well as any subsequent filings with the Securities and Exchange Commission. In addition, any forward-looking statements represent Prime Medicine’s views only as of today and should not be relied upon as representing its views as of any subsequent date. Prime Medicine explicitly disclaims any obligation to update any forward-looking statements subject to any obligations under applicable law. No representations or warranties (expressed or implied) are made about the accuracy of any such forward-looking statements.

Investor and Media Contacts

Gregory Dearborn
Prime Medicine
857-209-0696
gdearborn@primemedicine.com

Hannah Deresiewicz
Precision AQ
212-362-1200
hannah.deresiewicz@precisionaq.com

Condensed Consolidated Balance Sheet Data
(unaudited)

 
(in thousands) March 31,
2026
 December 31,
2025
 
Cash, cash equivalents, and investments $135,497 $177,680 
Total assets $294,730 $342,733 
Total liabilities $218,030 $221,865 
Total stockholders’ equity $76,700 $120,868 
 


Condensed Consolidated Statement of Operations
(unaudited)

 
  Three Months Ended
March 31,
 
(in thousands, except share and per share amounts) 2026
 2025
 
Revenue:         
Collaboration revenue — related party $856  $1,454  
Operating expenses:         
Research and development  34,105   40,562  
General and administrative  17,405   13,284  
Total operating expenses  51,510   53,846  
Loss from operations  (50,654)  (52,392) 
Other income:         
Interest income  1,021   1,182  
Accretion (amortization) of investments  460   339  
Change in fair value of short-term investment — related party     (1,056) 
Other income, net  51   37  
Total other income, net  1,532   502  
Net loss attributable to common stockholders $(49,122) $(51,890) 
Net loss per share attributable to common stockholders, basic and diluted $(0.28) $(0.40) 
Weighted-average common shares outstanding, basic and diluted  177,096,225   130,884,490  

FAQ

What did Prime Medicine (PRME) report for Q1 2026 net loss and cash position?

Prime Medicine reported a $49.1M net loss and $149.2M cash and investments as of March 31, 2026. According to Prime Medicine, the company expects this cash position to provide a runway into 2027 under current operating plans.

When will Prime Medicine (PRME) file IND/CTA for PM577 and PM647?

Prime Medicine expects to file an IND and/or CTA for PM577 in H1 2026 and for PM647 in mid-2026. According to Prime Medicine, initial clinical data for both programs are expected in 2027.

What is the status of PM359 (CGD) and potential BLA timeline for PRME?

Prime Medicine is engaging with the FDA toward a potential BLA filing for PM359 following positive proof-of-concept data from two patients. According to Prime Medicine, regulatory dialogue is ongoing and no BLA has been filed yet.

How did Prime Medicine's R&D and G&A expenses change in Q1 2026 versus Q1 2025?

R&D expenses decreased to $34.1M while G&A increased to $17.4M in Q1 2026. According to Prime Medicine, R&D reduction reflected strategic prioritization and workforce reductions, while G&A rose due to arbitration-related legal costs.

What does Prime Medicine (PRME) say about its clinical data timeline for Wilson Disease and AATD?

Prime Medicine expects initial clinical data in 2027 for its Wilson Disease (PM577) and AATD (PM647) programs. According to Prime Medicine, both programs are being advanced toward first-in-human studies after planned regulatory filings in 2026.