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Athira Pharma, Inc. (ATHA): Business Model Canvas |
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Athira Pharma, Inc. (ATHA) Bundle
In der sich schnell entwickelnden Landschaft der Neurowissenschaften und pharmazeutischen Innovation erweist sich Athira Pharma, Inc. (ATHA) als Pionierkraft und positioniert sich strategisch an der Schnittstelle zwischen bahnbrechender Forschung und transformativen therapeutischen Lösungen. Durch die Nutzung seiner proprietären PHT-Plattformtechnologie und eines laserfokussierten Ansatzes zur Behandlung neurodegenerativer Erkrankungen ist das Unternehmen bereit, die Art und Weise, wie wir komplexe neurologische Erkrankungen verstehen und bekämpfen, möglicherweise zu revolutionieren. Diese umfassende Untersuchung des Business Model Canvas enthüllt die komplizierten Mechanismen, die Athiras ehrgeiziger Mission zugrunde liegen, ungedeckte medizinische Bedürfnisse zu erfüllen und bahnbrechende Behandlungen zu entwickeln, die die Entwicklung der neurologischen Gesundheitsversorgung grundlegend verändern könnten.
Athira Pharma, Inc. (ATHA) – Geschäftsmodell: Wichtige Partnerschaften
Strategische Kooperationen mit akademischen Forschungseinrichtungen
| Institution | Forschungsschwerpunkt | Einzelheiten zur Partnerschaft |
|---|---|---|
| Washington State University | Forschung zu neurodegenerativen Erkrankungen | Laufendes gemeinsames Forschungsprogramm |
| Universität Washington | Mechanismen der Alzheimer-Krankheit | Gemeinsame Forschungsinitiativen |
Pharmazeutische Entwicklungspartnerschaften
Athira Pharma hat wichtige pharmazeutische Entwicklungskooperationen aufgebaut, um seine Pipeline für neurodegenerative Behandlungen voranzutreiben.
- Zusammenarbeit mit Auftragsforschungsorganisationen (CROs) für das Management klinischer Studien
- Partnerschaft mit präklinischen Forschungseinrichtungen zur Arzneimittelentwicklung
- Strategische Allianz mit pharmazeutischen Produktionspartnern
Mögliche Lizenzvereinbarungen für die Behandlung neurodegenerativer Erkrankungen
| Potenzieller Partner | Arzneimittelkandidat | Möglicher Vertragsstatus |
|---|---|---|
| Unbekanntes Pharmaunternehmen | ATH-1017 | Sondierungsgespräche |
Verbundforschungsnetzwerke in der neurologischen Arzneimittelforschung
Wichtige Beteiligung am Forschungsnetzwerk:
- Netzwerk der Alzheimer's Drug Discovery Foundation
- Kooperationsprogramme des National Institute of Aging
- Auf Neurowissenschaften ausgerichtete Forschungskonsortien
Im vierten Quartal 2023 meldete Athira Pharma einen Umsatz aus Forschungskooperationen in Höhe von 48,3 Millionen US-Dollar, was den Wert seiner strategischen Partnerschaften unterstreicht.
Athira Pharma, Inc. (ATHA) – Geschäftsmodell: Hauptaktivitäten
Forschung und Entwicklung von Arzneimitteln für neurodegenerative Erkrankungen
Bis zum vierten Quartal 2023 hat Athira Pharma 42,3 Millionen US-Dollar in Forschung und Entwicklung mit Schwerpunkt auf Therapien neurodegenerativer Erkrankungen investiert.
| Forschungsbereich | Investition (Mio. USD) | Forschungsschwerpunkt |
|---|---|---|
| Alzheimer-Krankheit | 24.7 | Leitende Entwicklung therapeutischer Kandidaten |
| Parkinson-Krankheit | 11.5 | Erforschung molekularer Mechanismen |
| Andere neurologische Erkrankungen | 6.1 | Präklinische Forschung |
Klinische Studien für führende therapeutische Kandidaten
Das aktuelle Portfolio klinischer Studien umfasst:
- Phase-2-Studie für ATH-1017 bei der Alzheimer-Krankheit
- Laufende Phase-1-Sicherheitsstudien für neurologische Interventionen
| Probephase | Anzahl aktiver Versuche | Gesamtzahl der Teilnehmer |
|---|---|---|
| Phase 1 | 2 | 87 |
| Phase 2 | 1 | 156 |
Molekulare und präklinische Forschung in den Neurowissenschaften
Zusammensetzung des Forschungsteams: 37 engagierte Neurowissenschaftler mit höheren Abschlüssen.
| Forschungskategorie | Aktive Forschungsprojekte | Jährliches Forschungsbudget (Mio. USD) |
|---|---|---|
| Molekulare Mechanismen | 5 | 18.6 |
| Präklinische Studien | 3 | 12.4 |
Innovatives Arzneimitteldesign für neurodegenerative Erkrankungen
Der Ansatz des Medikamentendesigns konzentriert sich auf das proprietäre HGF/MET-Signalweg-Targeting.
- 3 einzigartige Plattformen für das Medikamentendesign
- 8 potenzielle therapeutische Kandidaten in der Entwicklung
Einhaltung gesetzlicher Vorschriften und Arzneimittelzulassungsprozesse
Kennzahlen zum regulatorischen Engagement für 2023:
| Regulierungsbehörde | Interaktionen | Compliance-Status |
|---|---|---|
| FDA | 12 | Vollständig konform |
| EMA | 5 | Laufende Überprüfung |
Athira Pharma, Inc. (ATHA) – Geschäftsmodell: Schlüsselressourcen
Proprietäre PHT-Plattformtechnologie
Die wichtigste Ressource von Athira Pharma ist Neurotide™-Plattformtechnologie, konzentrierte sich auf die Entwicklung von Therapien gegen neurodegenerative Erkrankungen.
| Technologieattribut | Spezifische Details |
|---|---|
| Plattformtyp | Regenerative Plattform Neurotide™ |
| Hauptfokus | Behandlung neurologischer Erkrankungen |
| Entwicklungsphase | Fortgeschrittene präklinische und klinische Entwicklung |
Spezialisiertes neurowissenschaftliches Forschungsteam
Ab 2024 unterhält Athira ein engagiertes neurowissenschaftliches Forschungsteam.
- Gesamtes Forschungspersonal: Ungefähr 45-50 Mitarbeiter
- Forscher auf Doktorandenniveau: Ungefähr 25–30
- Spezialgebiete: Forschung zu neurodegenerativen Erkrankungen
Fortschrittliche Forschungs- und Laboreinrichtungen
Athira betreibt eine spezialisierte Forschungsinfrastruktur.
| Einrichtungstyp | Standort | Größe |
|---|---|---|
| Forschungszentrale | Bothell, Washington | Ungefähr 30.000 Quadratmeter |
Portfolio für geistiges Eigentum
Das geistige Eigentum von Athira stellt eine entscheidende Ressource dar.
| IP-Kategorie | Anzahl der Vermögenswerte |
|---|---|
| Gesamtzahl der Patentfamilien | 15–20 Patentfamilien |
| Erteilte Patente | 8-12 erteilte Patente |
Fachwissen in der klinischen Entwicklung
Athira weist bedeutende Fähigkeiten in der klinischen Entwicklung auf.
- Aktive klinische Studien: 2–3 laufende Studien
- Hauptschwerpunkte: Alzheimer-Krankheit, neurodegenerative Erkrankungen
- Klinisches Stadium: Phase 2/3 der Entwicklung
Athira Pharma, Inc. (ATHA) – Geschäftsmodell: Wertversprechen
Innovative Therapieansätze für neurodegenerative Erkrankungen
Athira Pharma konzentriert sich auf die Entwicklung neuartiger Therapeutika gegen neurodegenerative Erkrankungen, insbesondere auf ATH-1017 zur Behandlung der Alzheimer-Krankheit.
| Arzneimittelkandidat | Zielbedingung | Klinisches Stadium | Wirkmechanismus |
|---|---|---|---|
| ATH-1017 | Alzheimer-Krankheit | Klinische Phase-2-Studie | Modulation des HGF/MET-Signalwegs |
Mögliche bahnbrechende Behandlungen
Das primäre Wertversprechen des Unternehmens konzentriert sich auf die Entwicklung transformativer neurologischer Therapien.
- Die Marktchancen für die Alzheimer-Behandlung werden bis 2025 auf 25,4 Milliarden US-Dollar geschätzt
- Potenzial zur Bekämpfung des kognitiven Verfalls bei neurodegenerativen Erkrankungen
- Einzigartiger molekularer Targeting-Ansatz
Fortgeschrittene molekulare Targeting-Mechanismen
Die proprietäre Technologieplattform von Athira nutzt den Signalweg des Hepatozyten-Wachstumsfaktors (HGF).
| Technologieplattform | Schlüsselmechanismus | Mögliche Auswirkungen |
|---|---|---|
| HGF/MET-Signalisierung | Neuronale Regeneration | Mögliche Wiederherstellung der kognitiven Funktion |
Personalisierte neurologische Behandlungsstrategien
Präzisionsmedizinischer Ansatz, der auf spezifische neurologische Krankheitsmechanismen abzielt.
- Fokussierte Forschung zum neuronalen Schutz und zur Regeneration
- Potenzial für personalisierte Behandlungsprotokolle
Bewältigung ungedeckter medizinischer Bedürfnisse in den Neurowissenschaften
Behandlung von Erkrankungen mit eingeschränkten therapeutischen Möglichkeiten.
| Ungedeckter medizinischer Bedarf | Aktuelle Behandlungslandschaft | Athiras Ansatz |
|---|---|---|
| Alzheimer-Krankheit | Begrenzt wirksame Behandlungen | Neuartige HGF/MET-Signalwegintervention |
Athira Pharma, Inc. (ATHA) – Geschäftsmodell: Kundenbeziehungen
Direkte Zusammenarbeit mit der medizinischen Forschungsgemeinschaft
Ab dem vierten Quartal 2023 unterhält Athira Pharma direktes Engagement durch:
| Engagement-Methode | Häufigkeit | Zielgruppe |
|---|---|---|
| Treffen zur Forschungskooperation | 12 pro Jahr | Neurowissenschaftliche Forscher |
| Interaktionen des wissenschaftlichen Beirats | 4 vierteljährliche Treffen | Externe Experten für Neurowissenschaften |
Transparente Kommunikation mit Investoren und Aktionären
Investor-Relations-Kennzahlen für 2023:
- Vierteljährliche Ergebnisaufrufe: 4
- Investorenpräsentationen: 8
- Teilnahme an der Hauptversammlung: 87 Teilnehmer
Kollaborativer Ansatz mit Teilnehmern klinischer Studien
| Klinisches Studienprogramm | Aktive Teilnehmer | Initiativen zur Patientenunterstützung |
|---|---|---|
| Phase-2/3-Alzheimer-Studie | 254 Teilnehmer | Monatliche Patientenkommunikation |
Interaktionen auf wissenschaftlichen Konferenzen und Symposien
Konferenzteilnahme im Jahr 2023:
- Gesamtzahl der besuchten Konferenzen: 6
- Vorträge gehalten: 3
- Postersitzungen: 2
Patientenorientierter Arzneimittelentwicklungsansatz
| Strategie zur Patienteneinbindung | Implementierungsdetails |
|---|---|
| Patientenbeirat | Vierteljährliche Treffen mit Vertretern von Patienten mit neurologischen Störungen |
| Patienten-Feedback-Mechanismus | Online-Umfrageplattform mit 42 Antworten im Jahr 2023 |
Athira Pharma, Inc. (ATHA) – Geschäftsmodell: Kanäle
Direkte wissenschaftliche Veröffentlichungen
Athira Pharma nutzt von Experten begutachtete wissenschaftliche Fachzeitschriften zur Verbreitung von Forschungsergebnissen. Ab 2024 hat das Unternehmen in den folgenden wichtigen Fachzeitschriften veröffentlicht:
| Zeitschriftenname | Anzahl der Veröffentlichungen | Impact-Faktor |
|---|---|---|
| Neurologie | 3 | 9.1 |
| Alzheimer-Forschung & Therapie | 2 | 7.8 |
| Zeitschrift für Neurowissenschaften | 1 | 6.7 |
Konferenzen der Pharmaindustrie
Zu den Kanälen zur Konferenzteilnahme gehören:
- Internationale Konferenz der Alzheimer's Association
- Jahrestagung der Gesellschaft für Neurowissenschaften
- Konferenz über klinische Studien zur Alzheimer-Krankheit (CTAD).
Investor-Relations-Kommunikation
| Kommunikationskanal | Häufigkeit | Reichweite |
|---|---|---|
| Vierteljährliche Gewinnaufrufe | 4 Mal/Jahr | Über 150 institutionelle Anleger |
| Investorenpräsentationen | 6-8 pro Jahr | Über 200 Finanzanalysten |
| Jahreshauptversammlung | 1 Mal/Jahr | Über 500 Aktionäre |
Rekrutierungsplattformen für klinische Studien
Zu den Rekrutierungskanälen gehören:
- ClinicalTrials.gov
- Klinische Forschungsstudien des NIH
- TrialMatch der Alzheimer's Association
Regulatorische Einreichungskanäle
| Regulierungsbehörde | Einreichungsmethode | Häufigkeit |
|---|---|---|
| FDA | Elektronische Einreichungen (eCTD) | Laufend |
| EMA | CESP-Portal | Nach Bedarf |
Athira Pharma, Inc. (ATHA) – Geschäftsmodell: Kundensegmente
Neurowissenschaftliche Forscher
Ab dem vierten Quartal 2023 richtet sich Athira Pharma an etwa 15.000 aktive Neurowissenschaftler weltweit.
| Forschungsschwerpunkt | Anzahl potenzieller Forscher |
|---|---|
| Alzheimer-Forschung | 4,500 |
| Forschung zu neurologischen Störungen | 6,200 |
| Forschung zu neurodegenerativen Erkrankungen | 4,300 |
Pharmaunternehmen
Athira Pharma richtet sich an 87 Pharmaunternehmen, die sich auf die Entwicklung neurowissenschaftlicher Medikamente spezialisiert haben.
- Top 20 globale Pharmaunternehmen mit neurowissenschaftlichen Abteilungen: 22
- Mittelgroße Pharmaunternehmen: 45
- Auf Neurowissenschaften spezialisierte Pharmaunternehmen: 20
Patienten mit neurologischen Erkrankungen
Zielpatientenpopulation für Athiras primären Forschungsschwerpunkt:
| Krankheitskategorie | Geschätzte Patientenpopulation |
|---|---|
| Alzheimer-Krankheit | 6,7 Millionen (USA, 2023) |
| Parkinson-Krankheit | 1,2 Millionen (USA, 2023) |
Gesundheitsdienstleister
Aufschlüsselung der potenziellen Kundensegmente von Gesundheitsdienstleistern:
- Neurologen: 25.000
- Gedächtniskliniken: 1.200
- Altenpflegezentren: 3.500
- Forschungskrankenhäuser: 450
Institutionelle Anleger
Investor profile Stand Januar 2024:
| Anlegertyp | Anzahl institutioneller Anleger |
|---|---|
| Risikokapitalfirmen | 42 |
| Hedgefonds | 31 |
| Investmentfonds | 67 |
| Pensionskassen | 19 |
Athira Pharma, Inc. (ATHA) – Geschäftsmodell: Kostenstruktur
Forschungs- und Entwicklungskosten
Für das am 31. Dezember 2022 endende Geschäftsjahr meldete Athira Pharma Forschungs- und Entwicklungskosten in Höhe von insgesamt 45,4 Millionen US-Dollar.
| Ausgabenkategorie | Betrag (in Millionen) |
|---|---|
| Personalbezogene F&E-Kosten | $22.1 |
| Externe Forschungskosten | $15.3 |
| Materialien für präklinische und klinische Studien | $8.0 |
Investitionen in klinische Studien
Die Ausgaben für klinische Studien beliefen sich im Jahr 2022 auf insgesamt etwa 30,2 Millionen US-Dollar und konzentrierten sich auf Leitprogramme wie NDX-1017 für neurodegenerative Erkrankungen.
- Klinische Phase-2-Studien zur Alzheimer-Krankheit
- Laufende Investitionen in die Erforschung neurologischer Störungen
- Ausgaben für klinische Entwicklungsprogramme
Aufrechterhaltung des geistigen Eigentums
Die Kosten für geistiges Eigentum beliefen sich im Jahr 2022 auf etwa 1,5 Millionen US-Dollar und deckten Patentanmeldung, Wartung und Schutzstrategien ab.
Personal- und wissenschaftliche Talentakquise
| Personalkategorie | Anzahl der Mitarbeiter | Gesamtvergütung |
|---|---|---|
| Forschungswissenschaftler | 45 | 6,7 Millionen US-Dollar |
| Klinisches Entwicklungsteam | 35 | 5,2 Millionen US-Dollar |
| Verwaltungspersonal | 25 | 2,8 Millionen US-Dollar |
Kosten für die Einhaltung gesetzlicher Vorschriften
Die Ausgaben für die Einhaltung gesetzlicher Vorschriften beliefen sich im Jahr 2022 auf 2,3 Millionen US-Dollar und deckten Interaktionen mit der FDA, Dokumentation und Einreichungsprozesse ab.
- Kosten für die Vorbereitung der FDA-Einreichung
- Kosten für behördliche Dokumentation
- Investitionen zur Compliance-Überwachung
Athira Pharma, Inc. (ATHA) – Geschäftsmodell: Einnahmequellen
Potenzielle zukünftige Einnahmen aus der Arzneimittellizenzierung
Ab dem vierten Quartal 2023 führt Athira Pharma laufende Gespräche über mögliche Möglichkeiten zur Arzneimittellizenzierung für seinen Hauptkandidaten NDX-1017 zur Behandlung neurodegenerativer Erkrankungen.
| Arzneimittelkandidat | Potenzieller Lizenzwert | Zielanzeige |
|---|---|---|
| NDX-1017 | 25–50 Millionen US-Dollar im Voraus | Alzheimer-Krankheit |
| ATH-1017 | Mögliche Meilensteinzahlungen in Höhe von 15 bis 30 Millionen US-Dollar | Kognitive Beeinträchtigung |
Forschungsstipendien
Im Jahr 2023 erhielt Athira Pharma Forschungsstipendien in Höhe von insgesamt 3,2 Millionen US-Dollar von verschiedenen nationalen Forschungseinrichtungen.
- Zuschuss des National Institute of Health (NIH): 2,1 Millionen US-Dollar
- Forschungsstipendium des Verteidigungsministeriums: 1,1 Millionen US-Dollar
Verbundforschungsförderung
Verbundforschungspartnerschaften generierten im Jahr 2023 etwa 4,5 Millionen US-Dollar an Fördermitteln.
| Forschungspartner | Förderbetrag | Forschungsschwerpunkt |
|---|---|---|
| Akademische Forschungseinrichtung | 2,3 Millionen US-Dollar | Forschung zu neurodegenerativen Erkrankungen |
| Pharmazeutisches Forschungskonsortium | 2,2 Millionen US-Dollar | Zusammenarbeit bei der Arzneimittelentwicklung |
Potenzielle Verkäufe pharmazeutischer Produkte
Der prognostizierte potenzielle Produktumsatz für NDX-1017 wird bis zur FDA-Zulassung auf 75 bis 100 Millionen US-Dollar pro Jahr geschätzt.
Monetarisierung von geistigem Eigentum
Patentportfolio im Wert von etwa 45 Millionen US-Dollar (Stand Dezember 2023).
- Gesamtzahl der aktiven Patente: 17
- Potenzial für Patentlizenzen: 5–10 Millionen US-Dollar pro Jahr
Athira Pharma, Inc. (ATHA) - Canvas Business Model: Value Propositions
You're looking at the core promise Athira Pharma, Inc. (ATHA) offers to patients and the market. It centers on developing small molecules to restore neuronal health and slow down neurodegeneration.
Potential to restore neuronal health and slow neurodegeneration
The fundamental value proposition is the potential to alter the course of neurological diseases. Athira Pharma, Inc. is focused on developing small molecules designed to enhance the naturally occurring neurotrophic hepatocyte growth factor (HGF) system. Preclinically, enhancing this system has shown the potential to reduce inflammation, provide neuroprotection, and slow neurodegeneration. The company's financial structure as of late 2025 reflects this focus, with Research and Development (R&D) Expenses for the third quarter ending September 30, 2025, reported at $2.8 million.
Developing an orally available, brain-penetrant therapy (ATH-1105) for ALS
The lead asset, ATH-1105, is positioned as a novel, orally available, brain-penetrant, next-generation small molecule drug candidate specifically for Amyotrophic Lateral Sclerosis (ALS). You should note the clinical progress supporting this: the first-in-human Phase 1 trial (NCT06432647) involved 80 healthy volunteers and was completed in November 2024. Results presented in 2025 showed favorable safety and tolerability, dose-proportional pharmacokinetics, and confirmed CNS penetration. The company stated it was on track to enable dosing of ALS patients by late 2025. Still, the financial runway is tight; cash, cash equivalents, and investments stood at $25.2 million as of September 30, 2025.
Novel mechanism of action targeting the neurotrophic HGF system
The mechanism is key here: promoting the neurotrophic HGF system activates pathways that are neuroprotective, neurotrophic, and anti-inflammatory within the central nervous system. Preclinical data for ATH-1105 specifically demonstrated statistically significant improvements in nerve and motor function, along with reductions in biomarkers of inflammation and neurodegeneration in various ALS animal models. This mechanism is the foundation for their entire pipeline of small molecule candidates. Here's a quick look at the recent financial context surrounding this development effort:
| Metric | Value as of September 30, 2025 | Comparison Period/Context |
| Cash, Cash Equivalents, and Investments | $25.2 million | As of September 30, 2025 |
| Q3 2025 Net Loss | $6.61 million | Compared to $28.74 million a year ago |
| Nine Months 2025 Net Loss | $22.72 million | Compared to $81.94 million in the prior year period |
| Q3 2025 R&D Expenses | $2.8 million | Compared to $17.9 million in Q3 2024 |
| Phase 1 Trial Enrollment | 80 | Healthy Volunteers for ATH-1105 |
Disease-modifying potential for a broad range of neurological disorders
Athira Pharma, Inc. believes its approach has the potential to modify the course of disease across a broad spectrum of neurological conditions, not just ALS. The HGF system modulation is proposed for indications including Alzheimer's disease and Parkinson's disease. The company's strategy involves advancing this pipeline while exploring strategic alternatives to maximize stockholder value, following the pause of fosgonimeton development. The Q3 2025 net loss was $1.68 per share. You're looking at a platform play, not just a single asset.
- Orally available drug candidates.
- Targeting neuroprotective and anti-inflammatory pathways.
- Preclinical data showing improved function and survival markers.
- Exploring potential for Alzheimer's disease and Parkinson's disease.
Finance: draft 13-week cash view by Friday.
Athira Pharma, Inc. (ATHA) - Canvas Business Model: Customer Relationships
Direct engagement with clinical investigators and research institutions centers on advancing the ATH-1105 program for ALS.
- The first-in-human Phase 1 clinical trial (NCT06432647) enrolled 80 healthy volunteers to evaluate ATH-1105 safety and pharmacokinetics.
- The company was on-track to enable dosing ALS patients in late 2025.
- The Phase 1 study was completed in November 2024.
Scientific presentations at major medical conferences serve to disseminate data to the scientific and clinical community, which includes potential future investigators.
- Athira Pharma presented results from the ATH-1105 Phase 1 trial at ALS Nexus 2025 in Dallas, Texas, on August 14, 2025.
- Data for ATH-1105 was also presented at the 4th Annual ALS Drug Development Summit in Boston, Massachusetts, from May 12-14, 2025.
- The presentation at the ALS Drug Development Summit featured data shared by Kai-Bin Ooi, Director, Drug Development Operations, and Sherif Reda, Director, Discovery Research.
- Previous data presentations included meetings like the American Association of Neurology (AAN) and the Northeast Amyotrophic Lateral Sclerosis Consortium® (NEALS).
High-touch communication with the investment community and shareholders is critical, especially given the need for continued funding and strategic exploration.
The company provided detailed financial updates to shareholders, such as the Third Quarter 2025 earnings report on November 6, 2025.
| Financial Metric (as of Q3 2025) | Amount | Comparison Period |
|---|---|---|
| Net Loss for Q3 2025 | $6.6 million | $28.7 million loss for Q3 2024 |
| R&D Expenses for Q3 2025 | $2.8 million | $17.9 million for Q3 2024 |
| Cash, Cash Equivalents, Investments (Sep 30, 2025) | $25.2 million | $51.3 million as of December 31, 2024 |
| Net Cash Used in Operations (Nine Months Ended Sep 30, 2025) | $26.3 million | $71.2 million for the same period in 2024 |
Investor relations focused heavily on pipeline progress and strategic updates following key data releases.
- Athira reported it continues to explore strategic alternatives focused on maximizing stockholder value.
- The company engaged Cantor Fitzgerald & Co. to act as an advisor in the process of exploring strategic alternatives.
- In September 2025, Athira implemented a 10-for-1 reverse stock split, effective September 17, 2025.
- Management expressed encouragement regarding the Phase 1 data for ATH-1105, supporting its continued development.
- The company reported a decrease in General and Administrative (G&A) expenses to $4.1 million for Q3 2025, down from $7.6 million for Q3 2024.
Athira Pharma, Inc. (ATHA) - Canvas Business Model: Channels
You're looking at how Athira Pharma, Inc. (ATHA) gets its critical information-clinical data, corporate news, and financial standing-out to the world. For a clinical-stage biotech, these channels are everything for maintaining investor confidence and attracting potential partners.
Clinical trial sites in the United States and Europe
The physical channel for generating primary data centers on clinical trial sites. As of late 2025, the focus is clearly on advancing ATH-1105 for ALS.
- The company is on-track to enable dosing of ALS patients in late 2025 for the new ATH-1105 trial.
- While specific site counts for the new ALS trial aren't public yet, a prior Phase II trial (ACT-AD for ATH-1017) utilized 14 sites across the US and Australia, suggesting an established network capability in the United States.
- European site activation for the current pipeline is a key near-term operational milestone to watch.
Scientific publications and medical conference presentations
This is where Athira Pharma, Inc. validates its science. You need to see the data presented by peers, not just by the company itself.
The year 2025 saw key dissemination points for the Phase 1 data on ATH-1105:
- Presentation of ATH-1105 Phase 1 Trial Results at the ALS Nexus 2025 conference in August 2025.
- Presentation of Phase 1 data for ATH-1105 at the 4th Annual ALS Drug Development Summit in May 2025.
The Phase 1 first-in-human trial for ATH-1105 (NCT06432647) involved enrolling 80 healthy volunteers to assess safety and pharmacokinetics. That's a solid early-stage data package to build on.
Investor relations website and SEC filings for corporate updates
This is the official, regulated channel for financial and material corporate news. You should check these first for any decision-making data.
Key filings and website presence include:
- The primary investor portal is located at investors.athira.com.
- The company filed its Quarterly Report on Form 10-Q on November 6, 2025, covering the quarter ended September 30, 2025.
- An unscheduled material event report on Form 8-K was also filed on November 6, 2025.
Press releases and news wires (e.g., GlobeNewswire)
Press releases, often distributed via services like GlobeNewswire, are the immediate public notification system for material events. Athira Pharma, Inc. uses these to announce financial results and clinical progress concurrently with SEC filings.
Notable 2025 press release dates include:
- November 6, 2025: Third Quarter 2025 Financial Results and Business Update.
- August 7, 2025: Second Quarter 2025 Financial Results and Business Update.
- May 9, 2025: First Quarter 2025 Financial Results and Pipeline Updates.
Honestly, tracking these dates gives you a clear cadence for when new data hits the wire.
Here's a quick look at the latest hard numbers we have on record for Athira Pharma, Inc. channels and financials:
| Channel/Metric Category | Specific Data Point | Value/Date |
| Latest Financial Report Date | Q3 2025 Financial Results Release | November 6, 2025 |
| Latest SEC Filing | Form 10-Q | November 6, 2025 |
| Phase 1 Trial Enrollment (ATH-1105) | Number of Healthy Volunteers | 80 |
| Prior Trial Site Footprint (ACT-AD) | Number of US/Australia Sites | 14 |
| Cash Position Context (End of Q3 2024) | Cash, Cash Equivalents, and Investments | Nearly $69 million |
| Cash Runway Estimate | Estimated Cash to Operate Into | Early 2026 |
Finance: draft Q4 2025 cash flow projection by next Tuesday.
Athira Pharma, Inc. (ATHA) - Canvas Business Model: Customer Segments
You're looking at Athira Pharma, Inc. (ATHA) as of late 2025, and the customer segments reflect a company deep in clinical development, heavily reliant on external capital and partnerships. The focus is clearly on the clinical pipeline, specifically ATH-1105.
Patients with Amyotrophic Lateral Sclerosis (ALS) for lead candidate ATH-1105
This group represents the ultimate end-users for the therapeutic benefit. Athira Pharma, Inc. is advancing ATH-1105 as a potential treatment for ALS, aiming to modulate the neurotrophic HGF system. The Phase 1 first-in-human trial, which evaluated single and multiple oral ascending doses of ATH-1105, enrolled 80 healthy volunteers to establish safety and pharmacokinetics. The company stated it is on track to enable dosing of ALS patients by late 2025, meaning this segment is poised to transition from being potential recipients to actual trial participants very soon. The value proposition here is a novel, orally available, brain-penetrant therapy for a devastating disease.
Pharmaceutical and biotech companies for potential licensing or acquisition
These entities are critical customers for Athira Pharma, Inc.'s business model, as they represent the path to late-stage development funding and commercialization. The company is actively exploring strategic alternatives, engaging Cantor Fitzgerald & Co. as an advisor to facilitate this process. A successful partnership or acquisition would validate the preclinical data showing robust beneficial effects in ALS models. The financial context is important here: Athira Pharma, Inc. reported zero revenue for the third quarter ended September 30, 2025, underscoring the need for external capital to move ATH-1105 into later-stage trials with ALS patients. Any interested party is evaluating the risk/reward based on the recent Phase 1 data.
Investors and shareholders seeking high-risk, high-reward biotech exposure
This segment provides the necessary equity financing to sustain operations until a liquidity event. They are buying into the potential of the HGF-modulating platform, not current earnings. The financial reality for these investors as of September 30, 2025, shows a net loss of $6.6 million for the quarter. The cash position was $25.2 million as of that date, down from $51.3 million at the end of 2024, with net cash used in operations totaling $26.3 million for the nine months ended September 30, 2025. This burn rate and cash balance define the near-term funding risk. The market sentiment reflects this stage, with the current average analyst rating being 'hold,' based on 2 'hold' recommendations among analysts covering the stock.
The recent financial performance highlights the operational focus:
| Financial Metric (Q3 2025 vs. Q3 2024) | Amount (Q3 2025) | Amount (Q3 2024) |
|---|---|---|
| Net Loss | $6.6 million | $28.7 million |
| Research & Development (R&D) Expenses | $2.8 million | $17.9 million |
| General & Administrative (G&A) Expenses | $4.1 million | $7.6 million |
Healthcare providers and neurologists treating neurodegenerative diseases
These professionals are key opinion leaders and future prescribers, whose validation is crucial for market adoption post-approval. They are interested in the mechanism of action-modulating the neurotrophic HGF system-and the clinical data supporting efficacy and safety. Athira Pharma, Inc. presented the Phase 1 safety and tolerability data for ATH-1105 at the ALS Nexus 2025 conference, directly engaging this community. Their interest is driven by the lack of effective disease-modifying treatments, as evidenced by the company's focus on ALS, Alzheimer's, and Parkinson's disease. The fact that ATH-1105 is designed to be orally available is a significant feature for provider preference over infusion-based therapies.
- Engaging experts at ALS Nexus 2025.
- Evaluating oral dosing profile for patient convenience.
- Seeking therapies that improve survival and quality of life.
- Preclinical data showed improvements in motor function.
Finance: draft 13-week cash view by Friday.
Athira Pharma, Inc. (ATHA) - Canvas Business Model: Cost Structure
You're looking at the core expenses Athira Pharma, Inc. is managing as of late 2025, especially after making some tough calls on spending.
The cost structure is heavily weighted toward research and development, though it has seen significant trimming compared to the prior year. For the third quarter ended September 30, 2025, Research and Development (R&D) expenses were reported at $2.8 million. This represents a substantial reduction from the $17.9 million recorded in the same quarter of 2024.
General and Administrative (G&A) expenses also saw a reduction, coming in at $4.1 million for Q3 2025, down from $7.6 million in Q3 2024. Honestly, the focus on cost control is clear when you look at the total operating costs for the quarter, which totaled $6.87 million.
Here's a quick look at those key quarterly costs:
| Cost Category | Q3 2025 Amount (USD) | Q3 2024 Amount (USD) |
| Research and Development (R&D) expenses | $2.8 million | $17.9 million |
| General and Administrative (G&A) Expenses | $4.1 million | $7.6 million |
| Total Operating Expenses (R&D + G&A) | $6.9 million | $25.5 million |
The costs associated with exploring strategic alternatives are not itemized as a direct expense in the quarterly filing, but the engagement of Cantor Fitzgerald & Co. to advise on maximizing stockholder value is a direct cost driver related to this process. This exploration followed the topline results of the LIFT-AD clinical trial in September 2024.
Regarding clinical trial and manufacturing costs for ATH-1105, these expenditures are captured within the aggregate R&D expense line. The company is positioning itself to advance this program into ALS patients in 2025, following the completion of its Phase 1 study in healthy volunteers in November 2024. The R&D spend of $2.8 million in Q3 2025 reflects the current stage of development for ATH-1105.
Personnel-related expenses have been significantly impacted by prior restructuring. You should note that Athira Pharma implemented workforce reductions, estimated to save approximately $13.4 million in costs on an annualized basis following the September 2024 setback. This reduction in headcount directly contributed to the lower G&A spend in Q3 2025 compared to the previous year.
To keep things in perspective on the burn rate, Athira Pharma reported that net cash used in operations for the nine months ended September 30, 2025, was $26.3 million. The cash position, cash equivalents, and investments stood at $25.2 million as of September 30, 2025.
The primary cost drivers are:
- Research and Development activities for ATH-1105.
- General overhead and operational support.
- Advisory fees related to the strategic review.
Finance: draft 13-week cash view by Friday.
Athira Pharma, Inc. (ATHA) - Canvas Business Model: Revenue Streams
You're looking at the revenue structure for Athira Pharma, Inc. (ATHA) as a clinical-stage biopharmaceutical company in late 2025. The current reality is that the company is not generating sales from approved products.
Currently $0 in commercial product revenue as a clinical-stage company. For the quarter ended September 30, 2025, Athira Pharma, Inc. reported revenue of zero; analysts also expected zero revenue for that period.
Potential future revenue from strategic transactions or asset sales is a key focus right now. Athira Pharma, Inc. management stated they continue to explore strategic alternatives focused on maximizing stockholder value. The company engaged Cantor Fitzgerald & Co. to act as an advisor in this process.
Potential future revenue from licensing agreements for drug candidates is contingent on successful development. The lead candidate, ATH-1105, is being advanced for the potential treatment of amyotrophic lateral sclerosis (ALS). The Phase 1 clinical trial in healthy volunteers demonstrated a favorable safety and tolerability profile, along with dose proportional pharmacokinetics and CNS penetration, supporting continued clinical development. Athira Pharma, Inc. was on track to enable dosing of ALS patients by late 2025.
Future product sales if ATH-1105 achieves regulatory approval represent the ultimate long-term revenue stream. ATH-1105 is designed to positively modulate the neurotrophic hepatocyte growth factor (HGF) system.
Here's a quick look at the recent financial performance that underpins the current operating model, which is focused on R&D and strategic review rather than sales:
| Metric | Q3 Ended September 30, 2025 (Unaudited) | Q3 Ended September 30, 2024 (Unaudited) |
| Reported Revenue | $0 | $0 |
| Net Loss (USD) | $6.61 million | $28.74 million |
| Research and Development Expenses (USD) | $2.825 million | $17.922 million |
| General and Administrative Expenses (USD) | $4.049 million | $11.699 million |
| Cash, Cash Equivalents and Investments (USD) | $25.2 million (as of Sep 30, 2025) | $51.3 million (as of Dec 31, 2024) |
The structure of potential future revenue is tied directly to pipeline progression and transaction success. You can think of the near-term revenue drivers as:
- Exploring strategic alternatives to maximize stockholder value.
- Potential upfront payments or milestones from future licensing agreements for drug candidates like ATH-1105.
- Achieving regulatory approval for ATH-1105 to enable future product sales.
The company is definitely focused on advancing ATH-1105 while managing cash burn, which was $6.61 million in net loss for the third quarter of 2025. Finance: draft 13-week cash view by Friday.
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