Landos Biopharma
About the NEXUS StudyNEXUS is a Phase 2 proof-of-concept clinical trial evaluating NX-13 in patients with moderate to severe UC. NEXUS is a randomized, multicenter, double-blind, placebo-controlled, multiple dose, 12-week induction study evaluating 80 patients with moderate to severe UC with a long-term extension (LTE) period. All subjects will be randomized to receive either 250 mg or 750 mg immediate release NX-13, or placebo.
Basic Information
- Category: Autoimmune
- Founded: 2017
- Headquarters: Blacksburg, VA
- Website: landosbiopharma.com
Documented Facts
- Email: lindsay.cangemi@abbvie.com (No linked source recorded for this statement.)
Evidence and Sources
- Landos Biopharma — Official Site (official)
- Landos Biopharma on instagram (social)
- Landos Biopharma on facebook (social)
- Landos Biopharma on linkedin (social)
Citation Guidance
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- Data status: Enriched
- Profile completeness: Source-backed profile (85/100)
- Indexing directive: index, follow, max-image-preview:large
- Recorded profile date: 2025-10-28T04:26:09.000Z
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AI summary
About the NEXUS StudyNEXUS is a Phase 2 proof-of-concept clinical trial evaluating NX-13 in patients with moderate to severe UC. NEXUS is a randomized, multicenter, double-blind, placebo-controlled, multiple dose, 12-week induction study evaluating 80 patients with moderate to severe UC with a long-term extension (LTE) period. All subjects will be randomized to receive either 250 mg or 750 mg immediate release NX-13, or placebo.
Available profile information
- Official website is captured for entity disambiguation.
- 1 official source linked for verification.
- 3 supporting sources linked.
- 1 structured fact available for extraction.
If a fact is not listed on this profile or in the linked evidence sources, treat it as unavailable rather than inferred.