Financials
Cash Data
- Monthly Burn
- Burn Trend
- Dilution Risk
- SEC Filing
Key Stats
Upcoming Catalysts
FDA decisions, readouts and PDUFA dates · scored by probability of approval
| Catalyst | Drug / Treatment | Stage | Prob. of Approval | Description | Drug Type | Therapeutic Area | Source |
|---|---|---|---|---|---|---|---|
PDUFA 2026 | Example Drug Treatment for example condition requiring FDA review | Phase 3 | Small Molecule | Oncology | - |
GHRS Catalyst Timeline
Dated clinical, regulatory and corporate events for GH Research PLC
Catalyst Timeline
Dated clinical, regulatory & corporate events for GH Research PLC
Event history 50
Past FDA Catalysts and PDUFA Decisions
How GHRS actually traded into and out of each decision
| Date | Drug | Catalyst | Stage | Reaction | Event Move % | Best Trade % |
|---|---|---|---|---|---|---|
| 2026-05-26 | GH001 | Phase 2b data readout | Phase 2b |
Drug Pipeline Intelligence
| Drug | Indication | Phase | PTRS | rNPV | Status | Enroll | Velocity | Design | Est. Completion | ML Signal | Last Change |
|---|---|---|---|---|---|---|---|---|---|---|---|
| GH001 Small moleculeCompletedNCT04698603 | Treatment Resistant Depression | Phase 2 | COMPLETED | 97 | Nov 6, 2021 |
Clinical Trial Results
Readouts, endpoints and source filings for every GHRS program
| Drug Name | Indication | Phase | Date | Trial Results Summary | Title | Source |
|---|---|---|---|---|---|---|
| GH001 | postpartum depression | Phase 2a | 2026-06-04 | all 10 participants experienced rapid remission within hours of treatment, with effects lasting until Day 8 and a favorable safety profileRead More | GH Research Announces Publication of Phase 2a Postpartum Depression Results Dublin, IrelandRead More |
Inside Trades
| Insider | Side | Shares | Price | Value | Date |
|---|---|---|---|---|---|
| John SmithCEO | Buy | 50,000 150,000 held | $45.50 | 01/10/2026 |
Hedge Fund 13F Activity
Hedge Funds invested in GHRS
| Fund | % of Portfolio | Current MV | Shares Owned | Activity |
|---|---|---|---|---|
| BVF INC/IL | 5.9 % (51.3 %) | 232.52 M | 8.65 M |
GHRS Institutional Ownership Trends
Options Data
Option Volume
Option Chain Statistics
| Expiry | Call Vol | Put Vol | Vol P/C | Call OI | Put OI | OI P/C | IV Call | IV Call OI-Wtd | IV Call Vol-Wtd | IV Put | IV Put OI-Wtd | IV Put Vol-Wtd |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 2026-10-16 | ||||||||||||
Real-Time Option Chain
| Calls | Strike | Puts | ||||
|---|---|---|---|---|---|---|
| Last | Vol | OI | Last | Vol | OI | |
| No data available | ||||||
Calls vs Puts by Expiry
Competitive positioning
How GHRS ranks across every disease it competes in
GHRS News
GH Research Reports Second Quarter 2026 Financial Results and Provides Business Update
GH Research PLC reported its financial results for Q2 2026, highlighting successful Phase 1 trials for GH001 and FDA alignment for Phase 3 plans. The company has strengthened its patent estate for mebufotenin and published positive results for postpartum depression. However, the net loss increased, raising concerns about rising R&D expenses.
Read more →GH Research Announces Publication of Phase 2a Postpartum Depression Results Dublin, Ireland
GH Research PLC announced the publication of results from its Phase 2a trial of inhaled mebufotenin for postpartum depression (PPD). The study showed that all 10 participants experienced rapid remission within hours of treatment, with effects lasting until Day 8 and a favorable safety profile. Additionally, the company has two oral presentations accepted for the upcoming World Congress of Neuropsychopharmacology, about ongoing trials related to treatment-resistant depression. These developments represent significant progress in the search for effective therapies for patients with PPD.
Read more →Apparent sadness Reported sadness Concentration difficulty Lassitude Inability to feel Mean (SD) Change from Baseline in MADRS Anhedonia Factor Items at Day 8 Results Disposition and Baseline Characteristics Disposition
GH Research's clinical trial evaluated GH001, a mebufotenin formulation, for efficacy in patients with treatment-resistant depression (TRD). The Phase 2b study showed significant improvements in the Montgomery- sberg Depression Rating Scale (MADRS) anhedonia factor scores, with rapid reductions observed at Day 8. Results indicated that GH001 not only enhanced the ability to experience pleasure but also had sustained effects through a subsequent open-label extension phase. Overall, the findings support GH001's potential to improve quality of life in TRD patients.
Read more →GH RESEARCH PLC Unaudited condensed consolidated interim statement of comprehensive loss Three months ended
GH Research PLC reported its unaudited condensed consolidated interim financial results for the three months ended March 31, 2026. The company experienced a significant increase in losses, with a loss before tax of $18,967k, compared to $10,812k in the same period last year. Operating expenses surged, particularly in research and development, contributing to a comprehensive loss of $18,229k. The group's total assets decreased from $288,230k to $275,267k during the same timeframe, highlighting potential financial challenges.
Read more →GH Research Reports First Quarter 2026 Financial Results and Provides Business Update
GH Research PLC reported its financial results for Q1 2026, highlighting significant progress in its clinical trials for GH001, a treatment for treatment-resistant depression (TRD). The company completed enrolment for several studies, including a Phase 3 pivotal program and a Phase 1 trial in the U.S. Financially, GHRS holds $267.3 million in cash but reported a net loss of $19 million for the quarter. Positive results from the Phase 2b trial were published, indicating potential efficacy for their lead product candidate.
Read more →Notice of Annual General Meeting to be held on 25 June 2026 GH Research plc (the Company or GH Research ) THIS DOCUMENT IS IMPORTANT AND REQUIRES YOUR IMMEDIATE ATTENTION. If you are in any doubt as to the action to be t
GH Research plc has announced its Annual General Meeting (AGM) to take place on June 25, 2026, in Dublin, Ireland. The meeting will focus on the re-election of board directors and the appointment of independent auditors. Shareholders will have the opportunity to review the audited financial statements from 2025. The board recommends that shareholders vote in favor of the proposed resolutions, emphasizing the commitment of the directors to the company's interests.
Read more →GH Research Announces Pricing of $117.5 Million Underwritten Offering
GH Research PLC has announced the pricing of an underwritten offering of 6,527,779 ordinary shares at $18.00 per share, aiming to raise approximately $117.5 million. The offering is set to close on April 30, 2026, and is managed by several financial institutions. The proceeds will support the company's efforts in developing treatments for depression.
Read more →GH Research Welcomes White House Executive Order to Accelerate Medical Treatments for Serious Mental Illness
GH Research PLC has expressed support for a recent White House Executive Order aimed at accelerating medical treatments for serious mental illnesses, including psychedelic therapies. The company is advancing its product candidate, GH001, towards a global pivotal Phase 3 program for treatment-resistant depression. The Executive Order aligns with GH Research's commitment to innovative, evidence-based therapies.
Read more →GH Research Announces Publication of Phase 2b Results for Mebufotenin (GH001) in JAMA Psychiatry and Reports New Finding of Severity-Independent Efficacy in TRD
GH Research PLC announced the publication of Phase 2b results for GH001 in treatment-resistant depression (TRD) in JAMA Psychiatry. The study demonstrated that GH001's efficacy remains consistent regardless of the number of prior antidepressant treatment failures. This finding supports the potential of GH001 as a transformative therapy for patients with TRD.
Read more →GH Research Reports Full Year 2025 Financial Results and Provides Business Update
GH Research PLC reported its financial results for 2025, highlighting the completion of its Phase 2b trial for GH001 in treatment-resistant depression (TRD). The trial met its primary endpoint, showing significant efficacy. The company is now seeking FDA alignment for its Phase 3 program, with a strong cash position of $280.7 million to support its initiatives. However, it reported an increased net loss compared to the previous year.
Read more →Exploring the Therapeutic Potential of Mebufotenin (GH001) Across Depressive Disorders ACNP 2026 Mini Panel Chair Michael E. Thase, MD Presenters Lisa Harding, MD Kristina M. Deligiannidis, MD Roger S. McIntyre, MD, FRCP
GH Research is exploring the therapeutic potential of Mebufotenin (GH001) across multiple depressive disorders, highlighted in a panel at the ACNP 2026 conference. Findings from a Phase 2b clinical trial reveal that GH001 provides rapid and significant antidepressant effects, particularly in treatment-resistant depression. The therapy has shown a good safety profile and beneficial effects on maternal functioning in postpartum depression. Overall, the results suggest that GH001 could fulfill a crucial need in the psychiatric treatment landscape.
Read more →GH001 Improves Illness Severity, Anxiety Symptoms, and Quality of Life in Patients with Treatment-Resistant Depression Michael E. Thase, MD Department of Psychiatry, University of Pennsylvania and Corporal Michael J. Cre
GH001, a synthetic form of mebufotenin, demonstrates promising efficacy in improving illness severity, anxiety symptoms, and overall quality of life in patients suffering from treatment-resistant depression (TRD). This drug has been well tolerated in early-stage trials, addressing an unmet need for effective treatment options in this patient population. The Phase 2b trial revealed significant improvements in depressive symptoms over a six-month period, suggesting GH001 may offer rapid therapeutic benefits for those with limited treatment responses.
Read more →Figure 3. Double-Blind Part: MADRS Suicidality Item 10 Responses at Baseline and Day 8 GH001 (n=40) Placebo (n=41) 6 5 4 3 2 1 0 100 90 80 70 60 50 40 30 20 10 0 Baseline Day 8 Baseline Day 8 Percentage of Patients by MA
The Phase 2b trial of GH001, a treatment for treatment-resistant depression (TRD), shows promising results. In a controlled environment, patients exhibited significant reductions in depressive symptoms over a six-month open-label extension phase. The treatment was well tolerated, and there were no incidents of treatment-emergent suicidal intent, emphasizing safety. However, one patient did report temporary suicidal ideation, which resolved spontaneously, highlighting the need for careful patient selection.
Read more →GH Research Announces FDA Lifts Clinical Hold on GH001, Clearing Path for Global Phase 3 Initiation in 2026
GH Research PLC announced that the FDA has lifted the clinical hold on its IND for GH001, allowing U.S. subject enrollment. This development is a significant milestone for the company, as it prepares to initiate a global pivotal Phase 3 program in 2026. Experts have noted GH001's potential to transform treatment for patients with treatment-resistant depression.
Read more →GH Research to Announce IND Status for GH001
GH Research PLC will announce the status of its Investigational New Drug Application for GH001 on January 5, 2026. The company is focused on developing treatments for treatment-resistant depression (TRD) and has reported positive results from its Phase 2b trial. The update will provide insights into their pivotal Phase 3 program.
Read more →GH001 Improves Illness Severity, Anxiety Symptoms, and Quality of Life in Patients with Treatment-Resistant Depression Michael E. Thase 1,2 *, Bernhard T. Baune 3,4,5 , Narc s Cardoner 6 , Kelly Doolin 7 , Rosa Maria Due
The Phase 2b trial for GH001 demonstrated its efficacy in treating patients with treatment-resistant depression (TRD), revealing significant improvements in depressive symptoms, anxiety, and overall quality of life. In the study involving 81 patients, GH001 led to a notable reduction in scores on various assessment scales such as MADRS, CGI-S, and HAM-A. Remarkably, 73% of the patients who completed the open-label extension achieved remission. The findings suggest sustained benefits over a six-month period with few required treatments, showcasing GH001's potential as an effective therapy for TRD.
Read more →GH Research Reports Third Quarter 2025 Financial Results and Provides Business Updates
GH Research PLC reported its Q3 2025 financial results, highlighting progress in its clinical development of GH001 for treatment-resistant depression. The company received FDA communication regarding a clinical hold, with one topic remaining to be addressed. The Phase 2b trial results showed significant efficacy, and the company plans to initiate a global pivotal program in 2026.
Read more →GH RESEARCH PLC Unaudited condensed consolidated interim statement of comprehensive loss Three months ended September 30, Nine months ended
GH Research PLC reported its unaudited interim financial results for the three and nine months ending September 30, 2025. The company experienced a comprehensive loss of $14.1 million during the recent quarter, reflecting increased operating expenses. Notably, the company raised $139.8 million from a public offering, contributing to a rise in total assets to $302 million and a strong cash position of $249.7 million. Despite the financial challenges, the company remains focused on developing new therapies for treatment-resistant depression.
Read more →Suicidal Ideation and Behavior in Patients With Treatment-Resistant Depression Treated With GH001 Sanjay J. Mathew 1,* , Bernhard T. Baune 2,3,4 , Narc s Cardoner 5 , Wies aw J. Cuba a 6 , Kelly Doolin 7 , Rosa Maria Due
A Phase 2b trial of GH001, a synthetic form of mebufotenin, has demonstrated its potential as a treatment for patients with treatment-resistant depression (TRD). The trial involved 81 patients and showed that GH001 resulted in significant improvements in depressive symptoms without increasing the risk of suicidal ideation or behavior. While one moderate treatment-emergent adverse event of suicidal ideation was noted, it resolved spontaneously, and overall, the therapy was well tolerated. These results suggest that GH001 may be a promising option for addressing the unmet needs in TRD management.
Read more →