NASDAQ$PRLD

Prelude Therapeutics Inc · Q3 2024 earnings

Q3 2024 earnings · · Investor relations

Briefing

Reported third quarter financial results and provided a corporate update.

Prelude Therapeutics reported its third quarter financial results, highlighting the clinical proof of concept for PRT3789, its IV SMARCA2 degrader, and the initiation of a Phase 1 trial for PRT7732, its oral SMARCA2 degrader. The company's cash runway extends into 2026, with $153.6 million in cash, cash equivalents, and marketable securities as of September 30, 2024.

  • Demonstrated clinical proof of concept with PRT3789, its IV SMARCA2 degrader.
  • Initiated a Phase 1 trial for PRT7732, its oral SMARCA2 degrader.
  • Presented first preclinical data from its next generation degrader antibody conjugate (Precision ADC) platform
  • Interim phase 1 clinical data with potentially best-in-class CDK9 inhibitor, PRT2527, in hematological malignancies to be presented at the American Society of Hematology Annual Meeting in December 2024

Headline financials

Total Revenue

$3M

No prior period
EPS

-$0.43

Previous: -$0.45+4.4%
Cash Runway (Qtrs)

2.0K

No prior period
Capital Expenditures

-$711K

Previous: -$591K-20.3%
Free Cash Flow

-$33M

Previous: -$26.3M-25.5%
Net Income

-$32.3M

Previous: -$30.6M-5.4%
Operating Income

-$34.4M

Previous: -$33.4M-3.0%
Cash & Equivalents

$11.1M

Previous: $231M-95.2%
Total Assets

$197M

Previous: $259M-23.7%
R&D Expense

$29.5M

Previous: $26.3M+12.2%
Stock-Based Comp

$5.93M

Previous: $6.72M-11.7%

Revenue & EPS history

Prelude Therapeutics · Revenue · Quarterly

$3M

Q3 2024
Beat estimate in 0 of 1 quarters(0%)
ActualEstimate

Forward guidance

Prelude Therapeutics anticipates continued progress in its clinical development programs, including completing monotherapy dose escalation for PRT3789, advancing PRT7732, and presenting interim clinical data for PRT2527.

Tailwinds

  • Completing monotherapy dose escalation for PRT3789 by year-end 2024.
  • Advancing PRT3789 into the next phase of development, initially in NSCLC and esophageal cancers.
  • Continuing enrollment in the PRT3789 combination study with docetaxel.
  • Reporting progress on PRT7732 beginning early 2025.
  • Presenting interim clinical data for PRT2527 at the American Society of Hematology Annual Meeting in December 2024.

Headwinds

  • Clinical trial outcomes are inherently uncertain.
  • Potential delays in enrollment of eligible patients.
  • Risks related to supply chain and manufacturing facilities.
  • Uncertainties in achieving development goals.
  • Dependence on ability to fund development activities.

Historical earnings impact

How earnings announcements have historically affected this stock's price.

Avg. return before/after earnings

Based on 19 quarterly earnings reports · overlaid with Q3 2024

Historical avgQ3 2024

+5.5%

Avg return

Earnings day

+6.7%

Avg return

5 days after

+5.1%

Avg return

30 days after

50%

11 / 22 earnings

Positive

+37.0%

Q4 2023

Best reaction

-8.2%

Q3 2022

Worst reaction

Earnings price reactions
QuarterReport dateReaction (Day 0)+5 days+30 days
Q1 2026-3.1%-6.7%-14.2%
Q4 2025+5.8%-6.7%+13.3%
Q3 2025+10.7%+22.2%+26.7%
Q1 2025-4.1%-2.5%+2.5%
Q4 2024+4.1%+1.7%+14.4%
Q3 2024-1.6%-7.8%-26.0%
Q2 2024+21.6%+2.2%-2.0%
Q1 2024-6.3%-2.6%-1.3%
Q4 2023+37.0%+23.1%+40.2%
Q3 2023+30.8%+74.6%+90.8%
Q2 2023-2.1%-4.8%-2.4%
Q1 2023-3.8%+3.4%-12.3%
Q4 2022+9.2%+12.0%+35.1%
Q3 2022-8.2%-12.5%-38.8%
Q2 2022+21.7%+32.4%+21.2%
Q1 2022+1.0%+15.5%+22.0%
Q4 2021+16.9%+3.1%-16.4%
Q3 2021-5.4%-6.5%-17.7%
Q2 2021-5.3%-5.7%-3.4%
Q1 2021+8.8%+3.3%-21.3%
Q4 2020-2.6%-5.4%-41.3%
Q3 2020-3.4%+15.3%+43.4%
Q2 2020
Q1 2020
Q4 2019
Q3 2019
Q2 2019
Q1 2019

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