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S-3 Filing
Seelos Therapeutics (SEELQ) S-3Shelf registration
Filed: 18 Dec 23, 4:54pm
| Nevada (State or other jurisdiction of incorporation or organization) | | | 87-0449967 (I.R.S. Employer Identification Number) | |
| Large accelerated filer ☐ | | | Accelerated filer ☐ | |
| Non-accelerated filer ☒ | | | Smaller reporting company ☒ | |
| | | | Emerging growth company ☐ | |
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Product | | | Indication | | | Development Phase | | | Development Status | |
SLS-002 Intranasal Racemic Ketamine | | | Acute Suicidal Ideation and Behavior (“ASIB”) in Major Depressive Disorder (“MDD”) | | | Phase II | | | Completed open-label patient enrollment and announced the initial topline data from Part 1 of the proof-of-concept (“PoC”) study on May 17, 2021; enrollment of Part 2 of a Phase II study closed in June 2023; topline data for Part 2 announced on September 20, 2023 | |
SLS-005 IV Trehalose | | | Amyotrophic Lateral Sclerosis (“ALS)” | | | Phase II/III | | | Completed enrollment of final participants in February 2023 in the registrational study; data readout expected in the first quarter of 2024 | |
| | | Spinocerebellar Ataxia (“SCA”) | | | Phase IIb/III | | | Announced dosing of the first participant in the registrational study in October 2022; enrollment of additional patients temporarily paused on March 29, 2023 | |
| | | Huntington’s Disease (“HD”) and Alzheimer’s Disease (“AD”) | | | Phase II | | | Obtaining biomarker activity | |
Product | | | Indication | | | Development Phase | | | Development Status | |
SLS-004 Gene Therapy | | | Parkinson’s Disease (“PD”) | | | Pre-IND | | | Preclinical in vivo studies ongoing; announced partial results from a study demonstrating downregulation of α-synuclein in December 2022; currently analyzing data while temporarily pausing additional spend | |
SLS-007 Peptide Inhibitor | | | PD | | | Pre-IND | | | Preclinical study completed and analysis of the results ongoing; next steps for development of this program will be decided in concert with SLS-004 results and readouts, as both target the same pathway upstream; temporarily pausing additional spend | |
SLS-009 | | | HD, AD, ALS | | | Pre-IND | | | Preclinical in vivo studies ongoing | |
| SEC registration fee | | | | $ | 31,621.14 | | |
| FINRA filing fee | | | | | (1) | | |
| Legal fees and expenses | | | | | (1) | | |
| Printing fees and expenses | | | | | (1) | | |
| Accounting fees and expenses | | | | | (1) | | |
| Transfer agent fees and expenses | | | | | (1) | | |
| Warrant agent fees and expenses | | | | | (1) | | |
| Trustee fees and expenses | | | | | (1) | | |
| Miscellaneous fees and expenses | | | | | (1) | | |
| Total | | | | $ | (1) | | |
| Signature | | | Title | | | Date | |
| /s/ Raj Mehra, Ph.D. Raj Mehra, Ph.D. | | | President, Chief Executive Officer and Chairman of the Board (Principal Executive Officer) | | | December 18, 2023 | |
| /s/ Michael Golembiewski Michael Golembiewski | | | Chief Financial Officer (Principal Financial and Accounting Officer) | | | December 18, 2023 | |
| /s/ Margaret Dalesandro, Ph.D. Margaret Dalesandro, Ph.D. | | | Director | | | December 18, 2023 | |
| /s/ Brian Lian, Ph.D. Brian Lian, Ph.D. | | | Director | | | December 18, 2023 | |
| /s/ Daniel J. O’Connor, J.D. Daniel J. O’Connor, J.D. | | | Director | | | December 18, 2023 | |
| /s/ Richard W. Pascoe Richard W. Pascoe | | | Director | | | December 18, 2023 | |