Developer docs
API playgroundTry for free, no card

Search company profiles

Reunion Neuroscience

Full company profile

uuid0000481

Namestring
Reunion Neuroscience
Legal namestring
Reunion Neuroscience
Company typeenum
Private
Founded yearint
2019
Descriptiontext

Reunion Neuroscience is a clinical-stage biopharmaceutical company developing psychedelic-inspired neurotherapeutics for underserved mental health conditions. The company's lead candidate, luvesilocin (RE104), is being advanced across multiple neuropsychiatric indications — postpartum depression, adjustment disorder, and generalized anxiety disorder — with an FDA Breakthrough Therapy Designation granted in February 2026 for the postpartum depression program on the basis of positive Phase 2 RECONNECT data showing a 23.0-point reduction in MADRS depression score at Day 7 (p=0.0094) with effects observed as early as Day 1 and sustained through 28-day follow-up. A second pipeline candidate, RE245, has an IND filing planned for 2026, indicating active portfolio diversification beyond the lead asset.

The company's core technology centers on proprietary psychedelic-inspired drug design intended to deliver rapid antidepressant and anxiolytic efficacy with a short psychoactive experience, differentiated from conventional SSRIs that require weeks of dosing. Luvesilocin's profile — rapid onset combined with durability — is positioned against the unmet need for fast-acting treatments in postpartum depression and related indications. The company has completed an End of Phase 2 meeting with FDA, aligned on the registrational path, and plans to initiate a pivotal Phase 3 trial in 2026.

Reunion Neuroscience is pre-revenue and funds operations through equity capital, most recently closing a $133 million Series A financing in September 2025 led by MPM Capital and Novo Holdings, with participation from Arkin Bio Ventures, FemHealth Ventures, Mitsui Global Investment, Palo Santo Fund, and Plaisance Capital Management. The company intends to generate revenue through prescription pharmaceutical sales following FDA approval, distributing via specialty pharmacies, hospitals, and healthcare providers, and has not disclosed any active out-licensing or partnership economics. Leadership transitioned in June 2026 with the appointment of Dr. Sahil V. Kirpekar, M.D., as President, CEO, and Board Member, bringing experience from atai Life Sciences and Otsuka Pharmaceutical relevant to late-stage clinical execution and potential strategic transactions.

Short descriptiontext

Reunion Neuroscience is a clinical-stage biopharmaceutical company developing psychedelic-inspired neurotherapeutics — led by luvesilocin (RE104) — for postpartum depression, adjustment disorder, and generalized anxiety disorder, with FDA Breakthrough Therapy Designation and a planned Phase 3 trial in 2026.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
1–10
akta.pro rankint
HeadquartersToronto, Canada
HQ citystring
Toronto
HQ countrystring
Canada
HQ regionstring
North America
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
neuropsychiatric therapeutics, psychedelic-inspired medicine, postpartum depression treatment, clinical-stage biopharmaceutical, mental health pharmaceuticals
Industry2 codes
1Rare Neurology & Neurodegenerative Disorder Therapies
CodeHLAIAIADPrimaryYes
2Neurology & CNS Specialty Pharmaceuticals
CodeHLAIACACPrimaryNo
NAICS code1 code
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
SIC code1 code
  • Services-Medical Laboratories8071
Product category
Neuropsychiatric Pharmaceuticals
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model1 record
1Pharmaceutical Product Revenue
TypeOne Time License
Description

Pre-revenue clinical-stage biotech company. Once drugs receive FDA approval, revenue will be generated through prescription pharmaceutical sales. The company is developing luvesilocin for postpartum depression with Breakthrough Therapy Designation accelerating the regulatory path.

globenewswire.com
Marketing channels3 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels1 record

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components4 values
Technology or R&D, Personnel, Marketing or Sales, Operations
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Core offering1 text field

Reunion Neuroscience is a clinical-stage biopharmaceutical company developing psychedelic-inspired neurotherapeutics for underserved mental health conditions. Its lead candidate, luvesilocin (RE104), is being advanced through clinical trials for postpartum depression, adjustment disorder, and generalized anxiety disorder, and has received FDA Breakthrough Therapy Designation for postpartum depression. A second pipeline candidate, RE245, is planned for IND filing in 2026.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 2 values shown
  • 23.0-point reduction in MADRS depression scale at Day 7 with 30mg dose (p=0.0094)
+1 more record
Product overview1 text field

Reunion Neuroscience is a clinical-stage biopharmaceutical company developing novel therapies for mental health conditions. The company's lead product is luvesilocin (RE104), a psychedelic-inspired therapeutic currently in Phase 2/3 development for postpartum depression, adjustment disorder, and generalized anxiety disorder. The company also has RE245 in its pipeline with an IND filing planned for 2026. The company completed a $133 million Series A financing to advance clinical development.

Product and service2 records
1Luvesilocin (RE104)
CategoryNeuropsychiatric Pharmaceutical
Description

Psychedelic-inspired neurotherapeutic in development as a prescription pharmaceutical for postpartum depression, adjustment disorder, and generalized anxiety disorder. Demonstrated a 23.0-point reduction in MADRS depression scale at Day 7 with 30mg dose (p=0.0094) in the Phase 2 RECONNECT trial in 84 adult female patients with moderate-to-severe postpartum depression, with effects observed as early as Day 1 and maintained through 28-day follow-up.

2RE245
CategoryNeuropsychiatric Pharmaceutical
Description

Investigational neuropsychiatric drug candidate intended to expand Reunion's pipeline beyond luvesilocin. IND filing planned for 2026.

Scale indicator3 records

Each record includes

Type, Value, Description, Source

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Peers10 records
TypeBroad incumbent
Description

Global CNS biopharma (developer of Abilify) and former employer of Reunion's new CEO. Large incumbent with established CNS commercial infrastructure relevant as a potential strategic partner for luvesilocin.

TypeDirect peer
Description

Developer of Zurzuvae (zuranolone) and Zulresso, the first FDA-approved therapies specifically for postpartum depression. Most directly comparable peer given same indication (PPD) and CNS specialty pharma model, though Sage is more advanced commercially.

TypeDirect peer
Description

Clinical-stage company developing psilocybin therapy for treatment-resistant depression, with Breakthrough Therapy Designation. Direct peer in psychedelic-inspired CNS drug development targeting depression.

TypeDirect peer
Description

Clinical-stage psychedelic medicine company developing MM-120 (lysergide) for anxiety disorders and other CNS indications. Direct peer in psychedelic-inspired therapeutics for anxiety and depression.

TypeDirect peer
Description

Clinical-stage biopharma developing psychedelic and psychedelic-inspired therapies for mental health, including depression and anxiety. Direct peer in psychedelic-inspired CNS development; also Reunion's incoming CEO's prior employer.

TypeDirect peer
Description

Clinical-stage company developing mebufotenin and other psychedelic-based therapies for treatment-resistant depression. Direct peer in psychedelic drug development for CNS indications.

TypeDirect peer
Description

Clinical-stage company developing deuterated psychedelic compounds (e.g., CYB003) for depression and other psychiatric conditions. Direct peer in psychedelic-inspired CNS therapeutics.

TypeBroad incumbent
Description

Large CNS-focused biopharmaceutical company that partnered with Sage Therapeutics on Zurzuvae/zuranolone for PPD. Broad incumbent with overlapping CNS franchise and commercial PPD presence that creates partnership and competitive overlap with Reunion.

TypeBroad incumbent
Description

Specialty CNS biopharma with franchises in epilepsy, psychiatry, and sleep. Broad incumbent in CNS specialty pharma that could compete for or partner on rapid-acting PPD/psychiatric assets.

TypeEmerging player
Description

Clinical-stage neuroscience company developing precision medicines for brain diseases including depression. Emerging player with overlapping CNS pipeline and similar Series-stage development profile.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat4 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Segment3 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile1 record

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
Yes
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature2 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles3 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds1 record

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors7 records

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Reunion Neuroscience

Neuropsychiatric Pharmaceuticalsreunionneuro.com

Reunion Neuroscience is a clinical-stage biopharmaceutical company developing psychedelic-inspired neurotherapeutics — led by luvesilocin (RE104) — for postpartum depression, adjustment disorder, and generalized anxiety disorder, with FDA Breakthrough Therapy Designation and a planned Phase 3 trial in 2026.

What Reunion Neuroscience does

Reunion Neuroscience is a clinical-stage biopharmaceutical company developing psychedelic-inspired neurotherapeutics for underserved mental health conditions. The company's lead candidate, luvesilocin (RE104), is being advanced across multiple neuropsychiatric indications — postpartum depression, adjustment disorder, and generalized anxiety disorder — with an FDA Breakthrough Therapy Designation granted in February 2026 for the postpartum depression program on the basis of positive Phase 2 RECONNECT data showing a 23.0-point reduction in MADRS depression score at Day 7 (p=0.0094) with effects observed as early as Day 1 and sustained through 28-day follow-up. A second pipeline candidate, RE245, has an IND filing planned for 2026, indicating active portfolio diversification beyond the lead asset.

The company's core technology centers on proprietary psychedelic-inspired drug design intended to deliver rapid antidepressant and anxiolytic efficacy with a short psychoactive experience, differentiated from conventional SSRIs that require weeks of dosing. Luvesilocin's profile — rapid onset combined with durability — is positioned against the unmet need for fast-acting treatments in postpartum depression and related indications. The company has completed an End of Phase 2 meeting with FDA, aligned on the registrational path, and plans to initiate a pivotal Phase 3 trial in 2026.

Reunion Neuroscience is pre-revenue and funds operations through equity capital, most recently closing a $133 million Series A financing in September 2025 led by MPM Capital and Novo Holdings, with participation from Arkin Bio Ventures, FemHealth Ventures, Mitsui Global Investment, Palo Santo Fund, and Plaisance Capital Management. The company intends to generate revenue through prescription pharmaceutical sales following FDA approval, distributing via specialty pharmacies, hospitals, and healthcare providers, and has not disclosed any active out-licensing or partnership economics. Leadership transitioned in June 2026 with the appointment of Dr. Sahil V. Kirpekar, M.D., as President, CEO, and Board Member, bringing experience from atai Life Sciences and Otsuka Pharmaceutical relevant to late-stage clinical execution and potential strategic transactions.

Reunion Neuroscience firmographics

Firmographics
Name
Reunion Neuroscience
Legal name
Reunion Neuroscience
Website
https://reunionneuro.com
Company type
Private
Founded year
2019
Operating status
Operating
Headcount range
1–10 employees
Short description
Reunion Neuroscience is a clinical-stage biopharmaceutical company developing psychedelic-inspired neurotherapeutics — led by luvesilocin (RE104) — for postpartum depression, adjustment disorder, and generalized anxiety disorder, with FDA Breakthrough Therapy Designation and a planned Phase 3 trial in 2026.
Ownership category
akta.pro rank

Reunion Neuroscience industry classification

Industry
Product category
Neuropsychiatric Pharmaceuticals
NAICS
Research and Development in Biotechnology (except Nanobiotechnology) (541714)
SIC
Services-Medical Laboratories (8071)
akta.pro primary industry
Rare Neurology & Neurodegenerative Disorder Therapies (HLAIAIAD)
akta.pro secondary industry
Neurology & CNS Specialty Pharmaceuticals (HLAIACAC)

Keywords

  • Neuropsychiatric therapeutics
  • Psychedelic-inspired medicine
  • Postpartum depression treatment
  • Clinical-stage biopharmaceutical
  • Mental health pharmaceuticals

Where Reunion Neuroscience is headquartered

Location

Headquarters

HQ city
Toronto
HQ country
Canada
HQ region
North America

Offices1 record

Markets served

Reunion Neuroscience business model

Business model
GTM type
B2B
Offering type
Hardware or Manufacturing
Cost components
Technology or R&D, Personnel, Marketing or Sales, Operations

Revenue model

  1. Pharmaceutical Product Revenue: Pre-revenue clinical-stage biotech company. Once drugs receive FDA approval, revenue will be generated through prescription pharmaceutical sales. The company is developing luvesilocin for postpartum depression with Breakthrough Therapy Designation accelerating the regulatory path.

Go-to-market motion1 record

Distribution channels1 record

Marketing channels3 records

Reunion Neuroscience product offering

Product offering

Core offering

Reunion Neuroscience is a clinical-stage biopharmaceutical company developing psychedelic-inspired neurotherapeutics for underserved mental health conditions. Its lead candidate, luvesilocin (RE104), is being advanced through clinical trials for postpartum depression, adjustment disorder, and generalized anxiety disorder, and has received FDA Breakthrough Therapy Designation for postpartum depression. A second pipeline candidate, RE245, is planned for IND filing in 2026.

Product overview

Reunion Neuroscience is a clinical-stage biopharmaceutical company developing novel therapies for mental health conditions. The company's lead product is luvesilocin (RE104), a psychedelic-inspired therapeutic currently in Phase 2/3 development for postpartum depression, adjustment disorder, and generalized anxiety disorder. The company also has RE245 in its pipeline with an IND filing planned for 2026. The company completed a $133 million Series A financing to advance clinical development.

Differentiator

Problem solved

Functional benefit

Products and services

  • Luvesilocin (RE104) Psychedelic-inspired neurotherapeutic in development as a prescription pharmaceutical for postpartum depression, adjustment disorder, and generalized anxiety disorder. Demonstrated a 23.0-point reduction in MADRS depression scale at Day 7 with 30mg dose (p=0.0094) in the Phase 2 RECONNECT trial in 84 adult female patients with moderate-to-severe postpartum depression, with effects observed as early as Day 1 and maintained through 28-day follow-up.
  • RE245 Investigational neuropsychiatric drug candidate intended to expand Reunion's pipeline beyond luvesilocin. IND filing planned for 2026.

Quantifiable outcome

  • 23.0-point reduction in MADRS depression scale at Day 7 with 30mg dose (p=0.0094)
  • +1 more outcomes

Companies that use Reunion Neuroscience

Customer profile

Segments3 records

Ideal customer profiles1 record

Reunion Neuroscience technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature2 records

Reunion Neuroscience partnerships and signals

Strategic signal

Scale indicators3 records

Recent moves6 records

Expansion highlights5 records

Reunion Neuroscience competitors and assessment

Company assessment

Broad incumbents

  • Otsuka Pharmaceutical: Global CNS biopharma (developer of Abilify) and former employer of Reunion's new CEO. Large incumbent with established CNS commercial infrastructure relevant as a potential strategic partner for luvesilocin.
  • Biogen: Large CNS-focused biopharmaceutical company that partnered with Sage Therapeutics on Zurzuvae/zuranolone for PPD. Broad incumbent with overlapping CNS franchise and commercial PPD presence that creates partnership and competitive overlap with Reunion.
  • Jazz Pharmaceuticals: Specialty CNS biopharma with franchises in epilepsy, psychiatry, and sleep. Broad incumbent in CNS specialty pharma that could compete for or partner on rapid-acting PPD/psychiatric assets.

Direct peers

  • Sage Therapeutics: Developer of Zurzuvae (zuranolone) and Zulresso, the first FDA-approved therapies specifically for postpartum depression. Most directly comparable peer given same indication (PPD) and CNS specialty pharma model, though Sage is more advanced commercially.
  • Compass Pathways: Clinical-stage company developing psilocybin therapy for treatment-resistant depression, with Breakthrough Therapy Designation. Direct peer in psychedelic-inspired CNS drug development targeting depression.
  • MindMed: Clinical-stage psychedelic medicine company developing MM-120 (lysergide) for anxiety disorders and other CNS indications. Direct peer in psychedelic-inspired therapeutics for anxiety and depression.
  • Atai Life Sciences: Clinical-stage biopharma developing psychedelic and psychedelic-inspired therapies for mental health, including depression and anxiety. Direct peer in psychedelic-inspired CNS development; also Reunion's incoming CEO's prior employer.
  • GH Research: Clinical-stage company developing mebufotenin and other psychedelic-based therapies for treatment-resistant depression. Direct peer in psychedelic drug development for CNS indications.
  • Cybin: Clinical-stage company developing deuterated psychedelic compounds (e.g., CYB003) for depression and other psychiatric conditions. Direct peer in psychedelic-inspired CNS therapeutics.

Emerging players

  • Neumora Therapeutics: Clinical-stage neuroscience company developing precision medicines for brain diseases including depression. Emerging player with overlapping CNS pipeline and similar Series-stage development profile.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat4 records

Key risks6 records

Key highlights7 records

Customer concentration

Reunion Neuroscience social profiles

Digital presence

Reunion Neuroscience financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Reunion Neuroscience leadership team

Management profile

Number of profiles

Profiles3 records

Reunion Neuroscience funding detail

Funding detail

Funding overview

Funding rounds1 record

Investors7 records

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

Reunion Neuroscience M&A and investment

M&A and investment

M&A

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about Reunion Neuroscience

What does Reunion Neuroscience do?

Reunion Neuroscience is a clinical-stage biopharmaceutical company developing psychedelic-inspired neurotherapeutics for underserved mental health conditions. Its lead candidate, luvesilocin (RE104), is being advanced through clinical trials for postpartum depression, adjustment disorder, and generalized anxiety disorder, and has received FDA Breakthrough Therapy Designation for postpartum depression. A second pipeline candidate, RE245, is planned for IND filing in 2026.

Is Reunion Neuroscience a public or private company?

Reunion Neuroscience is a private company. It is classified as venture growth investor backed and is currently operating.

When was Reunion Neuroscience founded?

Reunion Neuroscience was founded in 2019. It employs 1 to 10 people.

Where is Reunion Neuroscience based?

Reunion Neuroscience is headquartered in Toronto, Canada, in the North America region.

How does Reunion Neuroscience make money?

One revenue line is on record: pharmaceutical Product Revenue.

Who are Reunion Neuroscience's main competitors?

Broad incumbents on record are Otsuka Pharmaceutical, Biogen and Jazz Pharmaceuticals. Direct peers are Sage Therapeutics, Compass Pathways, MindMed, Atai Life Sciences, GH Research and Cybin. Neumora Therapeutics is listed as an emerging player.

Does Reunion Neuroscience have an API?

No public API is recorded for Reunion Neuroscience.

What industry is Reunion Neuroscience in?

Reunion Neuroscience's product category is Neuropsychiatric Pharmaceuticals. Its primary akta.pro industry code is HLAIAIAD, Rare Neurology & Neurodegenerative Disorder Therapies, with a secondary code of HLAIACAC, Neurology & CNS Specialty Pharmaceuticals. Its NAICS code is 541714 and its SIC code is 8071.

Unlock the full company data

50 free credits on sign-up, no credit card required.

Contact sales
Live signals
PR NewswirePostpartum Depression Market to Evolve During the Forecast Period (2026-2036) with Breakthrough Treatments and Expanding Pipeline Assets | DelveInsightThe postpartum depression treatment market is expected to grow through 2036, with the US leading in 2025. Approximately 1.3 million maternal PPD cases were diagnosed in the 7MM in 2025, and new therapies like Luvesilocin and LPCN 1154 are advancing in clinical trials.The Pharma LetterReunion Neuroscience names Sahil Kirpekar as new CEONew Jersey-based biotech company Reunion Neuroscience has appointed Dr. Sahil Kirpekar as its new president, CEO, and board member, effective immediately, succeeding Greg Mayes. Dr. Kirpekar is a physician with two decades of experience in health sciences, bringing expertise in commercial strategy, business development, capital markets, and clinical-stage value creation.citybizReunion Neuroscience Names Sahil Kirpekar President and CEOReunion Neuroscience has appointed Sahil V. Kirpekar as president, chief executive officer and board member, succeeding Greg Mayes who stepped down immediately. Kirpekar brings nearly two decades of experience in psychiatry and CNS disorders, including recent roles as chief business officer at Atai Life Sciences and global head of business development at Otsuka Pharmaceutical. The company is advancing its lead candidate luvesilocin across multiple psychiatric indications including postpartum depression, adjustment disorder and generalized anxiety disorder, with Phase 2 trials underway.GlobeNewswireReunion Neuroscience Announces Appointment of Sahil V. Kirpekar, M.D., as President and CEOReunion Neuroscience has appointed Sahil V. Kirpekar, M.D. as President, Chief Executive Officer, and a member of its Board of Directors, effective immediately, succeeding Greg Mayes. Dr. Kirpekar, a trained physician with two decades of experience in health sciences, joins from Atai Life Sciences where he served as Chief Business Officer, and brings a track record spanning several billion dollars in pharmaceutical transactions. The company is advancing its lead candidate luvesilocin in Phase 2 trials for postpartum depression, adjustment disorder, and generalized anxiety disorder, with a separate IND filing planned for RE245 in 2026.SubstackDispatch from The Netherlands Part 2The article reports on key takeaways from the ICPR psychedelics conference in Haarlem, highlighting discussions on negative clinical trial results for ketamine and psilocybin, which challenge assumptions about treatment efficacy. It also covers a cautionary panel on negligent homicide during an illegal psychedelic session and presentations on European ketamine clinics and novel treatments for postpartum depression by Reunion.GlobeNewswireReunion Neuroscience to Present Full Data from RECONNECT Phase 2 Clinical Trial at Upcoming ASCP and APA Annual MeetingsReunion Neuroscience announced it will present full data from its RECONNECT Phase 2 clinical trial evaluating luvesilocin for postpartum depression at the ASCP and APA Annual Meetings in 2026. The trial met its primary endpoint, demonstrating statistically significant and clinically meaningful reduction in depression symptoms as measured by MADRS score on Day 7, with effects maintained through 28-day follow-up. Based on these positive results, the FDA granted Breakthrough Therapy Designation and aligned on a registrational path, with the company expecting to advance luvesilocin into a pivotal Phase 3 trial in 2026.BioSpaceReunion Neuroscience to Present Full Data from RECONNECT Phase 2 Clinical Trial at Upcoming ASCP and APA Annual MeetingsReunion Neuroscience will present full RECONNECT Phase 2 trial data at the ASCP and APA meetings, showing a statistically significant reduction in postpartum depression symptoms. The trial met its primary endpoint, and the company aligned with the FDA on a registrational path, expecting a pivotal Phase 3 trial in 2026.GlobeNewswireU.S. FDA Grants Reunion Neuroscience’s Luvesilocin (RE104) Breakthrough Therapy Designation StatusThe U.S. FDA granted Breakthrough Therapy Designation to Reunion Neuroscience's luvesilocin for postpartum depression based on positive Phase 2 RECONNECT trial data showing statistically significant reduction in depression scores (p=0.0094). The trial demonstrated rapid and durable efficacy with 70% of patients achieving remission at both Day 7 and Day 28. The company is on track to initiate a pivotal Phase 3 trial in 2026.GlobeNewswireReunion Neuroscience to Participate in Upcoming Investor ConferencesReunion Neuroscience announced its participation in multiple upcoming investor conferences in February and March 2026, including Oppenheimer, TD Cowen, and others. The company will present on its lead product candidate RE104 for postpartum depression and other indications, and plans to file an IND for RE245 in 2026.GlobeNewswireReunion Neuroscience to Participate in Upcoming Investor ConferencesReunion Neuroscience, a clinical-stage biopharmaceutical company focused on mental health treatments, announced its participation in five upcoming investor conferences scheduled for February-March 2026, including the Oppenheimer Healthcare Life Sciences Conference, TD Cowen Healthcare Conference, and Leerink Partners Global Healthcare Conference. Members of the company's management team will host one-on-one investor meetings during each conference. The company is actively investigating its lead product candidate RE104 for postpartum depression, adjustment disorder, and generalized anxiety disorder, and plans to file an IND for another candidate, RE245, in 2026.