Prelude Therapeutics Incorporated (PRLD) Earnings

Prelude Therapeutics Incorporated is expected to report next earnings on August 13, 2026 (in NaN days), with a consensus EPS estimate of $-0.23. PRLD has beaten EPS estimates in 8 of its last 12 reported quarters (average surprise -120.1% over the last four).

Next earnings
Aug 13, 2026in NaN days
EPS est $-0.23 · Revenue est $5M
Track record
Beat EPS in 8 of 12 quarters
Avg surprise -120.1% (last 4 quarters)
Earnings history
Report dateEPS estEPS actualSurpriseRevenueRev. surprise
May 12, 2026$-0.27$-0.13+51.9%$5M+0.0%
Mar 10, 2026$-0.03$-0.20-566.7%$6M-72.5%
Nov 12, 2025$-0.35$-0.26+25.7%$7M-68.3%
Aug 14, 2025$-0.45$-0.41+8.9%
Mar 10, 2025$-0.49$-0.38+22.4%$4M
Feb 15, 2024$-0.50$-0.47+6.0%$3M
Nov 1, 2023$-0.58$-0.45+22.4%
Aug 3, 2023$-0.65$-0.54+16.9%
Mar 15, 2023$-0.63$-0.60+4.8%
Nov 14, 2022$-0.63$-0.63+0.0%
Mar 16, 2022$-0.69$-0.71-2.9%
Nov 12, 2021$-0.62$-0.66-6.5%

Source: company filings + earnings calendar. For informational purposes only — not investment advice.

Earnings call summary

Q4 FY2025 · March 10, 2026

AI summary of management’s prepared remarks and analyst Q&A. For informational purposes only — not investment advice.

Management highlights

Discussed aspects such as the clinical development plan for molecule 396 including a parallel design in myelofibrosis and polycythemia vera with input from key opinion leaders, the rationale behind choosing a degrader approach for CAT6 including selectivity and efficacy advantages, and work on the mutant Cal-R degrader with differentiation points like potency and potential for subcutaneous administration.

Guidance

Cash position was $106 million in cash, which takes the company into the second quarter of 2027, and this does not account for the potential $100 million option payment from Insight.

Segment performance

Not explicitly mentioned in detail

Risks & headwinds

Not discussed in detail

Analyst Q&A

  • Q: Can you differentiate your molecule from other competitors and why Insight would partner with you?

    A: Discussed selectivity profile, learnings from clinic/preclinical stages, and parallel clinical development plan.

  • Q: Talk about the clinical development plan for molecule 396?

    A: Parallel design in myelofibrosis and polycythemia vera, enrolling the right patients and getting FDA approval for the parallel approach.

  • Q: Talk about the CAT6 degrader?

    A: Differentiated by degrader approach for better selectivity and efficacy, plan to file IND by mid - year.

  • Q: What is the cash position?

    A: $106 million in cash, lasting into the second quarter of 2027