Prelude Therapeutics Incorporated (PRLD)

NASDAQ: PRLD · Real-Time Price · USD
4.700
+0.300 (6.82%)
At close: Apr 24, 2026, 4:00 PM EDT
4.710
+0.010 (0.21%)
After-hours: Apr 24, 2026, 7:51 PM EDT
Market Cap472.60M +835.7%
Revenue (ttm)12.14M +73.4%
Net Income-99.50M
EPS-1.29
Shares Out 100.55M
PE Ration/a
Forward PEn/a
Dividendn/a
Ex-Dividend Daten/a
Volume865,216
Open4.880
Previous Close4.400
Day's Range4.435 - 4.881
52-Week Range0.730 - 5.540
Beta0.72
AnalystsStrong Buy
Price Target4.67 (-0.64%)
Earnings DateMay 13, 2026

About PRLD

Prelude Therapeutics Incorporated, a clinical-stage precision oncology company, focuses on the discovery and development of novel precision cancer medicines to underserved patients. It is developing JAK2V617F, a driver mutation product for the treatment of myeloproliferative neoplasms, myelofibrosis (MF), polycythemia vera, and essential thrombocythemia (ET); KAT6A for the treatment of advanced breast cancer and other solid tumors; and mutated calreticulin degrader antibody conjugates to treat MF and ET. The company has collaboration with AbCel... [Read more]

Industry Biotechnology
Sector Healthcare
IPO Date Sep 25, 2020
Employees 79
Stock Exchange NASDAQ
Ticker Symbol PRLD
Full Company Profile

Financial Performance

In 2025, Prelude Therapeutics's revenue was $12.14 million, an increase of 73.43% compared to the previous year's $7.00 million. Losses were -$99.50 million, -21.76% less than in 2024.

Financial Statements

Analyst Summary

According to 3 analysts, the average rating for PRLD stock is "Strong Buy." The 12-month stock price target is $4.67, which is a decrease of -0.64% from the latest price.

Price Target
$4.67
(-0.64% downside)
Analyst Consensus: Strong Buy
Stock Forecasts

News

Prelude Therapeutics Announces Pricing of $90.0 Million Underwritten Offering

WILMINGTON, Del., April 20, 2026 (GLOBE NEWSWIRE) -- Prelude Therapeutics Incorporated (Nasdaq: PRLD) (“Prelude” or the “Company”), a clinical-stage precision oncology company, today announced the pri...

6 days ago - GlobeNewsWire

Prelude Therapeutics Presents Preclinical Data from Development Candidate, PRT13722, a First-in-Class, Orally Bioavailable, Potent and Highly Selective KAT6A Degrader at American Association for Cancer Research (AACR) Annual Meeting 2026

Data Demonstrate Potential for Differentiated Efficacy and Safety Profile, Including Complete Responses as Monotherapy in Multiple CDX and PDX Models of HR+/HER2- Breast Cancer

6 days ago - GlobeNewsWire

Prelude Therapeutics Announces the Appointment of Charles Morris, M.D. as Chief Medical Officer

WILMINGTON, Del., April 15, 2026 (GLOBE NEWSWIRE) -- Prelude Therapeutics Incorporated (Nasdaq: PRLD) (“Prelude Therapeutics” or the “Company”), a clinical-stage precision oncology company, today anno...

11 days ago - GlobeNewsWire

Prelude Therapeutics Announces Acceptance of Preclinical Abstract for PRT13722, a First-in-Class Oral KAT6A Selective Degrader at the 2026 AACR Annual Meeting

WILMINGTON, Del., March 17, 2026 (GLOBE NEWSWIRE) -- Prelude Therapeutics Incorporated (Nasdaq: PRLD), a precision oncology company, today announced that a poster with preclinical data on the Company'...

5 weeks ago - GlobeNewsWire

Prelude Therapeutics Transcript: Conference

The company has shifted its focus to JAK2V617F and KAT6A programs, targeting clinical entry in 2026, and is advancing a novel CALR degrader. Mutant-selective approaches and strategic partnerships, including a deal with Incyte, support a strong financial runway into 2027.

6 weeks ago - Transcripts

Prelude Therapeutics Reports Full Year 2025 Financial Results and Provides Program Outlook for 2026

Received FDA clearance of Investigational New Drug application (IND) for PRT12396, mutant-selective JAK2V617F inhibitor in the first quarter of 2026 Phase 1 study of PRT12396 in patients with polycyth...

6 weeks ago - GlobeNewsWire

Prelude Therapeutics Receives FDA Clearance of Investigational New Drug Application (IND) for PRT12396, a Mutant-selective JAK2V617F Inhibitor

WILMINGTON, Del., Feb. 03, 2026 (GLOBE NEWSWIRE) -- Prelude Therapeutics Incorporated (Nasdaq: PRLD), a precision oncology company, today announced that the U.S. Food and Drug Administration (FDA) cle...

2 months ago - GlobeNewsWire

Prelude Therapeutics Presents Data at the 2025 ASH Annual Meeting from its Myeloproliferative Neoplasm (MPN) Programs

First disclosure of PRT12396, a JAK2V617F-selective JH2 inhibitor demonstrates disease modifying potential in myeloproliferative neoplasms

5 months ago - GlobeNewsWire

PRLD Investors Have Opportunity to Join Prelude Therapeutics Incorporated Fraud Investigation with the Schall Law Firm

LOS ANGELES, Nov. 26, 2025 (GLOBE NEWSWIRE) -- The Schall Law Firm, a national shareholder rights litigation firm, announces that it is investigating claims on behalf of investors of Prelude Therapeut...

5 months ago - GlobeNewsWire

Prelude Therapeutics Earnings Call Transcript: Q3 2025

Secured $60M upfront and up to $910M in total from Incyte for the JAK2 V617F program, supporting clinical advancement of two lead oncology assets into 2026–2027. Both programs target large, high-need markets with differentiated, selective approaches and robust preclinical data.

5 months ago - Transcripts

Prelude Therapeutics Reports Third Quarter 2025 Financial Results and Provides Corporate Update

Lead candidate from mutant selective JAK2V617F JH2 inhibitor program advancing with IND filing expected in the first quarter of 2026

5 months ago - GlobeNewsWire

PRLD Investors Have Opportunity to Join Prelude Therapeutics Incorporated Fraud Investigation With the Schall Law Firm

LOS ANGELES--(BUSINESS WIRE)---- $PRLD--PRLD Investors Have Opportunity to Join Prelude Therapeutics Incorporated Fraud Investigation with the Schall Law Firm.

5 months ago - Business Wire

Prelude Therapeutics Announces Strategic Business Update

Prelude to prioritize development of mutant selective JAK2V617F JH2 inhibitor and KAT6A selective degrader programs Pausing further clinical development of SMARCA2 selective degrader programs JAK2V617...

6 months ago - GlobeNewsWire

Prelude Therapeutics Announces Exclusive Option Agreement with Incyte to Advance Mutant Selective JAK2V617F JH2 Inhibitors

Incyte secures an exclusive option to acquire Prelude's mutant selective JAK2V617F JH2 inhibitor program Mutant selective JAK2V617F JH2 inhibitors have disease-modifying potential in treating patients...

6 months ago - GlobeNewsWire

Prelude Therapeutics Announces Publication of Abstracts for Presentation at the American Society of Hematology 67th Annual Meeting

WILMINGTON, Del., Nov. 03, 2025 (GLOBE NEWSWIRE) -- Prelude Therapeutics Incorporated (Nasdaq: PRLD) (“Prelude” or the “Company”), a clinical-stage precision oncology company, today announced the publ...

6 months ago - GlobeNewsWire

Prelude Therapeutics Announces Appointment of Katina Dorton, J.D., MBA to its Board of Directors

WILMINGTON, Del., Oct. 17, 2025 (GLOBE NEWSWIRE) -- Prelude Therapeutics Incorporated (Nasdaq: PRLD), a clinical-stage precision oncology company, today announced the appointment of Katina Dorton to i...

6 months ago - GlobeNewsWire

Prelude Therapeutics Reports Second Quarter 2025 Financial Results and Provides Corporate Update

PRT7732, once daily oral SMARCA2 degrader, currently enrolling at the seventh dosing cohort (125 mg); Company to provide an update with preliminary clinical data, including PK/PD, safety and initial c...

9 months ago - GlobeNewsWire

Prelude Therapeutics Transcript: Goldman Sachs 46th Annual Global Healthcare Conference

Clinical programs for SMARCA2 degraders are advancing, with IV and oral agents showing promising efficacy and safety, especially in lung and upper GI cancers. The pipeline includes a selective CDK6 degrader and ADC collaborations, supported by a strong cash position into 2026.

11 months ago - Transcripts

Prelude Therapeutics Transcript: Jefferies Global Healthcare Conference 2025

Lead SMARCA2 programs show promising safety and efficacy, with both IV and oral candidates advancing quickly in aggressive cancer types. Pipeline expansion includes a selective CAT6A degrader and antibody conjugates, with strong preclinical data and new clinical milestones expected in 2024–2025.

11 months ago - Transcripts

Prelude Therapeutics to Participate in Upcoming Healthcare Conferences

WILMINGTON, Del., June 02, 2025 (GLOBE NEWSWIRE) -- Prelude Therapeutics Incorporated (Prelude) (Nasdaq: PRLD), a clinical-stage precision oncology company, announced today that the Company will parti...

11 months ago - GlobeNewsWire

Prelude Therapeutics Transcript: The Citizens JMP Life Sciences Conference 2025

Advancing SMARCA2 and KAT6A degrader programs, with strong early efficacy and rapid clinical progress. Oral and IV assets are being developed in parallel, supported by a solid cash position and active business development. Regulatory outlook remains positive.

1 year ago - Transcripts

Prelude Therapeutics Reports First Quarter 2025 Financial Results and Provides Corporate Update

PRT3789 monotherapy and combination with docetaxel escalation enrollment is complete and the Company plans to present updated results in the second half of 2025 Enrollment of the Phase 1 study of Prel...

1 year ago - GlobeNewsWire

Prelude Therapeutics to Participate in Citizens Life Sciences Conference

WILMINGTON, Del., May 01, 2025 (GLOBE NEWSWIRE) -- Prelude Therapeutics Incorporated (Prelude) (Nasdaq: PRLD), a clinical-stage precision oncology company, announced today that the Company will partic...

1 year ago - GlobeNewsWire

Prelude Announces Presentations at 2025 AACR Annual Meeting

Preclinical data elucidating the mechanism of action of PRT3789, Prelude's first-in-class, highly selective SMARCA2 degrader currently in early clinical development

1 year ago - GlobeNewsWire

Prelude Therapeutics Transcript: Barclays 27th Annual Global Healthcare Conference

Current macro and regulatory changes are not expected to disrupt operations, with proactive supply chain management in place. Lead SMARCA pathway degraders show promising early clinical results, and both IV and oral programs are advancing, with a major data update expected in H2 2025.

1 year ago - Transcripts