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US clinical-stage biopharmaceutical company developing intranasal racemic ketamine (SLS-002) for major depressive disorder with acute suicidal ideation and PTSD. Completed Phase 2 trials before filing for Chapter 11 bankruptcy in November 2024 and being delisted from Nasdaq; trading continues on OTCQB.

Development Programmes

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SLS-002 (Intranasal Racemic Ketamine)

Phase IIinactive

Acute suicidal ideation and behavior / MDD

Programme Tracker

Suicidality

Primary: US (FDA)
Phase IIinactive

Seelos filed Chapter 11 bankruptcy November 2024; assets acquired by GLD Partners for $22M (September 2025); GLD plans Phase 3 pivotal trials for SLS-002

Milestones

Efficacy data

Completed

Actual: Mar 1, 2024

SLS-005 (trehalose for ALS) trial missed primary endpoint

Why it matters: ALS trial failure precipitated Seelos's financial collapse. The company had invested heavily in SLS-005 alongside SLS-002, and the miss left insufficient capital to continue both programmes.

Company milestone

Completed

Actual: Nov 15, 2024

Seelos Therapeutics filed Chapter 11 bankruptcy in SDNY (Case 1:24-bk-11987); assets $0-$100K, liabilities $10M-$50M; Nasdaq delisted

Why it matters: Corporate death of Seelos Therapeutics. Despite having two INDs on file and Phase 2 data for SLS-002 (intranasal ketamine for suicidality), the company ran out of capital after the ALS trial failure.

Licensing deal

Completed

Actual: Sep 1, 2025

Bankruptcy court approved $22M credit bid sale to GLD Partners LP (Section 363 stalking horse sale)

Why it matters: GLD Partners acquired SLS-002 and SLS-005 assets at a significant discount to development cost. Section 363 sale provides clean title free of prior liabilities.

Licensing deal

Completed

Actual: Oct 21, 2025

GLD Partners completed acquisition of Seelos assets; announced plans for Phase 3 pivotal trials for both SLS-002 (ketamine/ASIB) and SLS-005 (trehalose/ALS with orphan drug pathway)

Why it matters: SLS-002 survives under new ownership. GLD Partners describes these as "late-stage assets with near-to mid-term value inflection points." If GLD is well-capitalized, SLS-002 could advance to Phase 3 for acute suicidal ideation — a critical unmet need where intranasal racemic ketamine could outperform Spravato (esketamine).

Watch next: GLD Partners Phase 3 trial design for SLS-002; new IND amendments; timeline for first patient enrolled under GLD

Recorded Events

Oct 21, 2025: Licensing deal

Sep 1, 2025: Licensing deal

Nov 15, 2024: Company milestone

Mar 1, 2024: Efficacy data

Quick Facts

Type
Public Biotech
Ticker
OTCQB: SEEL
Lead Stage
Phase II
Website
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Sponsored Trials

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