NASDAQ$GHRS

GH Research PLC · Q4 2025 earnings

Q4 2025 earnings · · Investor relations

Briefing

GH Research reported its full year 2025 financial results and provided a business update on its clinical-stage depression treatments.

GH Research, a clinical-stage biopharmaceutical company, reported a net loss of $48.3 million for the full year 2025. The company successfully completed its Phase 2b trial for GH001 in treatment-resistant depression, meeting its primary endpoint with significant MADRS reduction. The company maintains a strong cash position of $280.7 million to fund its upcoming Phase 3 pivotal program.

  • Phase 2b trial of GH001 met primary endpoint with a placebo-adjusted MADRS reduction of -15.5 points at Day 8 (p<0.0001).
  • GH001 achieved a 57.5% remission rate at Day 8 in the double-blind portion and 73% at six months in open-label extension.
  • FDA cleared GH001 for U.S. clinical investigation, enabling U.S. subject enrollment for the upcoming Phase 3 program.
  • Cash and marketable securities increased to $280.7 million following a successful capital raise during the year.

Headline financials

Total Revenue

$0.00

Previous: $0.00
EPS (adj)

$0.00

Previous: -$0.17+100.0%
MADRS Reduction

-15.5

No prior period
Remission Rate Day 8

57.5%

No prior period
R&D Expenses

$38.8M

No prior period
G&A Expenses

$22M

No prior period
6-Month Remission Rate

73.0%

No prior period
Net Income

$0.00

Previous: -$8.8M+100.0%
Operating Income

$0.00

Previous: -$12.9M+100.0%

Revenue & EPS history

GH Research · Revenue · Quarterly

$0

Q4 2025

Forward guidance

GH Research is focused on transitioning to a global Phase 3 pivotal program for GH001 and advancing its proprietary aerosol delivery device.

Tailwinds

  • Targeting initiation of global Phase 3 program in 2026.
  • Actively seeking FDA alignment on Phase 3 pivotal program design.
  • Proprietary aerosol delivery device Phase 1 trial ongoing to support bridging to pivotal trials.
  • Strong cash runway with $280.7 million in liquid assets.
  • GH001 cleared by FDA for U.S. clinical investigation.

Headwinds

  • Risk of delays in obtaining FDA alignment on pivotal program design.
  • Potential for future clinical holds by the FDA on GH001 or GH002.
  • Increasing R&D and G&A expenses as programs advance.
  • Uncertainty regarding the timeline for submitting an IND for GH002.
  • Dependence on successful replication of Phase 2b results in Phase 3 trials.

Historical earnings impact

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

Avg. return before/after earnings

Based on 10 quarterly earnings reports · overlaid with Q4 2025

Historical avgQ4 2025

+0.7%

Avg return

Earnings day

+1.4%

Avg return

5 days after

+0.7%

Avg return

30 days after

55%

6 / 11 earnings

Positive

+24.4%

Q3 2021

Best reaction

-19.3%

Q2 2024

Worst reaction

Earnings price reactions
QuarterReport dateReaction (Day 0)+5 days+30 days
Q1 2026+1.3%+0.2%
Q3 2025-1.2%+4.6%+9.6%
Q4 2025-4.8%-10.2%-21.6%
Q2 2025+2.2%+10.2%+19.3%
Q4 2024-2.9%-14.4%+0.8%
Q2 2024-19.3%-21.6%-37.8%
Q1 2024+4.5%+7.1%+25.9%
Q2 2023-5.8%+1.2%-5.0%
Q1 2023+8.2%+6.9%+24.6%
Q4 2021+1.1%+7.5%-15.6%
Q3 2021+24.4%+24.4%+7.1%
Q1 2021
Q4 2020
Q3 2020
Q2 2020
Q1 2020

Discussion

Share your read of this quarter. Sign-in carries your eToro identity.

Join the conversation

Sign in with eToro to post your read of this quarter and vote on others'.

Sign in with eToro