teleo-codex/entities/health/texas-impact-consortium.md
Teleo Agents e03015f06f vida: extract claims from 2025-12-12-utmb-uthealth-texas-ibogaine-impact-50m-oud
- Source: inbox/queue/2025-12-12-utmb-uthealth-texas-ibogaine-impact-50m-oud.md
- Domain: health
- Claims: 2, Entities: 1
- Enrichments: 2
- Extracted by: pipeline ingest (OpenRouter anthropic/claude-sonnet-4.5)

Pentagon-Agent: Vida <PIPELINE>
2026-05-11 04:21:51 +00:00

3 KiB

type entity_type name full_name domain status founded headquarters website tags
entity research_program Texas IMPACT Consortium Ibogaine Medicine for PTSD, Addiction, and Cognitive Trauma health active 2025-12 Texas, USA null
ibogaine
OUD
PTSD
TBI
psychedelic
clinical-trial
Texas

Overview

The Texas IMPACT (Ibogaine Medicine for PTSD, Addiction, and Cognitive Trauma) Consortium represents the largest state-sponsored psychedelic research investment in US history, with $50 million from Texas Health and Human Services Commission plus up to $50 million ARPA-H federal match for a potential $100 million total.

Structure

Lead institutions: UTHealth Houston and UTMB Health (Galveston)

Consortium members (11 institutions):

  • UTHealth Houston
  • UTMB Health
  • Texas Tech University
  • Texas Tech UTHS El Paso
  • UT Austin
  • UT Health Science Center San Antonio
  • UT Tyler
  • UT Rio Grande Valley
  • Texas A&M University
  • University of North Texas Health Science Center
  • Baylor College of Medicine
  • JPS Health Network (Dallas)

Research Design

Duration: Two-year multicenter trial (Phase 2 scale)

Conditions targeted:

  • Opioid use disorder (primary indication) — UTHealth Houston + UTMB
  • Traumatic brain injury — UT Austin + Baylor College of Medicine
  • PTSD — coordinated across sites

Key evidence basis:

  • Stanford 2024 study (n=30 veterans): 88% PTSD reduction, 87% depression reduction at 1 month
  • MAPS Phase 2 OUD: 70-75% abstinence at 1 month
  • Mechanism: Opioid receptor reset + GDNF production → dopaminergic neuron regeneration
  • Unique capability: Abolishes opioid withdrawal symptoms within 1-2 days

Regulatory Context

Current status: Ibogaine is Schedule I (federal) with no completed Phase 3 trial in US

Safety barrier: QT prolongation risk with >30 documented deaths in unsupervised settings

Political support:

  • Texas SB 2308 (December 2025): Authorized $50M state funding
  • Trump EO (April 2026): Directed ARPA-H funding toward ibogaine for veterans; DEA to initiate rescheduling upon Phase 3 completion
  • Colorado Proposition 122: Decriminalized in Colorado

Timeline

  • 2025-12 — Texas SB 2308 authorizes $50M state funding for IMPACT consortium
  • 2026-04 — Trump executive order directs ARPA-H to provide up to $50M federal match and commits DEA to rescheduling process upon Phase 3 completion

Significance

The Texas IMPACT consortium addresses the opioid overdose crisis (79,384 deaths in 2024), the most acute public health emergency in mental health/substance use. Ibogaine is the only psychedelic with credible single-session evidence for OUD specifically. The program demonstrates bipartisan political support through veteran-focused framing, with conservative Texas authorizing the largest state psychedelic research investment in US history.

Realistic FDA approval timeline: 2029-2030 if Phase 2 data supports Phase 3 advancement, making ibogaine 4-5 years behind psilocybin despite addressing higher-mortality condition.