Contineum Therapeutics
CTNMPhase 2Contineum Therapeutics leverages its expertise in neuro-immunology to develop next-generation therapies for complex diseases of the central nervous system and inflammatory conditions. The company's strategy centers on targeting specific receptor pathways implicated in disease progression, with its lead candidate, PIPE-307, in Phase 2 for multiple sclerosis and PIPE-791 in Phase 1 for idiopathic pulmonary fibrosis. Following its successful IPO in April 2024, Contineum is well-capitalized to advance its clinical pipeline and explore the therapeutic potential of its novel mechanisms of action.
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AI Company Overview
Contineum Therapeutics leverages its expertise in neuro-immunology to develop next-generation therapies for complex diseases of the central nervous system and inflammatory conditions. The company's strategy centers on targeting specific receptor pathways implicated in disease progression, with its lead candidate, PIPE-307, in Phase 2 for multiple sclerosis and PIPE-791 in Phase 1 for idiopathic pulmonary fibrosis. Following its successful IPO in April 2024, Contineum is well-capitalized to advance its clinical pipeline and explore the therapeutic potential of its novel mechanisms of action.
Technology Platform
Focused drug discovery on specific receptor pathways, particularly the lysophosphatidic acid 1 (LPA1) receptor and the muscarinic M1 receptor, to develop oral, brain-penetrant small molecule therapies for neuroinflammatory and fibrotic diseases.
Pipeline Snapshot
88 drugs in pipeline
| Drug | Indication | Stage | Watch |
|---|---|---|---|
| PIPE-791 Dose A + PIPE-791 Dose B + Placebo | Idiopathic Pulmonary Fibrosis | Phase 2 | |
| PIPE-307 Dose A + PIPE-307 Dose B + Placebo | Relapsing Remitting Multiple Sclerosis | Phase 2 | |
| PIPE-505 + Placebo | Sensorineural Hearing Loss | Phase 1/2 | |
| PIPE-791 | Idiopathic Pulmonary Fibrosis (IPF) | Phase 1 | |
| PIPE-307 | Multiple Sclerosis | Phase 1 |
Funding History
2Total raised: $190M
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Competitive Landscape
Contineum faces competition from established MS immunomodulators (e.g., Roche, Biogen) and IPF anti-fibrotics (e.g., Genentech, Boehringer Ingelheim). Its differentiation strategy is based on novel mechanisms (M1 modulation for remyelination, brain-penetrant LPA1 inhibition) that address unmet needs beyond current standards of care, targeting disease modification rather than just symptom management.
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