Vital Kauaʻi

Iboga in the United States

Directory

Companies, research centers, nonprofits and public offices active on ibogaine in the United States, each linked to its own site.

Last checked: October 26, 2026

Companies7

  • AtaiBeckley

    Psychedelic developer, a wholly owned subsidiary of Eli Lilly since 2026-09-11. atai formed an ibogaine joint venture with DemeRx in 2020; that venture, DemeRx IB, ran a UK Phase 1/2a study of oral ibogaine HCl (DMX-1002, cleared by the MHRA in 2021) and was acquired by atai, now AtaiBeckley, in November 2023. Lilly's lead acquired asset is BPL-003 (5-MeO-DMT). The current stage of an ibogaine program is not confirmed.

  • Beond

    Ibogaine treatment provider in Cancún that opened its U.S. headquarters in Austin in April 2026 for research, preparation and integration programs. No ibogaine is given at the Austin office.

    TX

  • Delix Therapeutics

    Neuroplastogen developer; zalsupindole (DLX-001) is a non-hallucinogenic 5-MeO-DMT analog, Phase 2 in depression expected Q4 2026. Not ibogaine-derived.

  • DemeRx

    Miami-based developer of DMX-1001 (oral noribogaine) for alcohol use disorder; IND accepted 2026-04-22; Phase 2 anticipated 2027. Independent of AtaiBeckley, which acquired the former DemeRx IB joint venture in November 2023.

    FL

  • Gilgamesh Pharma

    New York spinout formed when AbbVie agreed to acquire Gilgamesh Pharmaceuticals' bretisilocin (announced 2025-08-25); it kept the cardio-safe ibogaine analog for opioid use disorder (GM-3009, NIDA $14M), blixeprodil and the AbbVie collaboration. Phase 1 entry for the analog expected 2026 per report; closed a $60M Series A in March 2026.

    NY

  • Psyence BioMed

    Established Texas Ibogaine Research Corporation; investing up to $5M in PsyLabs (2026-09-23); holds a term sheet for US rights to PsyLabs pharmaceutical-grade ibogaine; partnered with DEA-registered Benuvia for planned US manufacture (2026-10-05).

    TX

  • Texas Ibogaine Research Corporation (Psyence BioMed)

    Texas subsidiary of Psyence BioMed that coordinates U.S. ibogaine licensing, supply and manufacturing and is planning a possible opioid use disorder trial.

    TX

Universities and research centers8

Clinics and trial sites2

Nonprofits and advocacy13

Government agencies24

Legislators and legislative offices24

Public voices12

  • Donald J. Trump

    President of the United States. Signed EO 14401 on 2026-04-18 and announced the University of Miami IND gift on 2026-08-18.

  • Robert F. Kennedy Jr.

    HHS Secretary. Attended EO signing; recipient of the 1994 ibogaine IND from the University of Miami.

  • Marty Makary

    Former FDA Commissioner. Attended the EO 14401 signing as FDA Commissioner; FDA issues vouchers and guidance under the order. He resigned on 2026-05-12, and Kyle Diamantas was named acting commissioner.

  • Rep. Morgan Luttrell

    U.S. Representative (R-TX), former Navy SEAL. Primary sponsor of the IBOGAINE Act (H.R. 9559) and co-author of the NDAA psychedelic amendments.

  • Rep. Michael McCaul

    U.S. Representative (R-TX). Cosponsor of the IBOGAINE Act (H.R. 9559) and backer of the NDAA amendments on veterans' neuroplastogen access.

  • Rick Perry

    Former Texas Governor. Co-launched the Texas Ibogaine Initiative; national voice for ibogaine research.

  • Greg Abbott

    Governor of Texas. Signed SB 2308 in June 2025 funding $50M ibogaine trials.

  • W. Bryan Hubbard

    CEO, Americans for Ibogaine. Attended EO signing; led Kentucky ibogaine effort and co-launched Texas initiative.

  • Nolan Williams, MD

    Late Stanford psychiatrist and neuroscientist (Brain Stimulation Lab). Led the Stanford ibogaine-magnesium veteran studies; died in October 2025.

  • Deborah Mash

    Founder and CEO, DemeRx. Developer of noribogaine DMX-1001, first FDA-accepted US ibogaine-derivative IND.

  • Doug Collins

    Secretary of Veterans Affairs. Named ibogaine as VA's next emphasis (2026-09-12); VA is working with FDA on Risk Evaluation and Mitigation Strategies for ibogaine's cardiac risks.

  • Betty Aldworth

    MAPS (Multidisciplinary Association for Psychedelic Studies). Told Reuters (2026-10-05), on FDA's ibogaine trial-design docket, that cardiac safety is the central challenge researchers must solve before ibogaine can responsibly reach the people who need it.

How this tracker is kept

  • Each state is checked against legislature records, agency releases and published reporting, and carries the date it was last checked. Every development links to its source.
  • “No known activity” means the state was checked on the date shown and no ibogaine-specific law, bill, funding or task force was found.
  • The directory lists organizations and public offices with their own websites. Listing points readers to them and does not endorse them.
  • This tracker is offered for education and does not constitute legal or medical advice. Ibogaine and iboga remain Schedule I substances under federal law. See the medical disclaimer.
  • To share a development or request a correction, write to aloha@vitalkauai.com. For daily coverage, see Iboga Worldwide.