Investigator View · TRL-0046

Investigator trial detail exposes startup, enrollment, and site execution context with deterministic metrics for portal planning. Regulated and operational boundaries remain labeled so users know which fields are informational versus workflow-driven. All portal actions are traceable through linked audit events and correlation IDs. Users can review study progression and align site readiness actions from a single governed page.

Type: Portal-onlyLast reviewed: 2026-02-19Owner: Medical AffairsStatus: Reviewed

Operational Queue

Monitor SLA-backed work items, pending approvals, and deterministic escalation rules.

Governed Actions

Submissions, exports, and AI runs are audit logged with correlation IDs and retention rules.

Portal Controls

Role constraints enforce ABAC-like behavior for content classes and workflow actions.

Page Focus

This child portal page emphasizes its dedicated operational detail content rather than section landing tiles.

LYA-221 durability study 46

Internal ID: TRL-0046

NCT-like: NCT90000045

Objective: Assess efficacy, safety, and patient-reported outcomes using a controlled synthetic protocol.

Endpoints: Primary endpoint is change from baseline at week 24 with key secondary safety measures.

Timeline: 2022-05-16 to 2026-05-16

Inclusion snapshot: protocol-defined adults with condition-specific disease activity and baseline laboratory eligibility.

Exclusion snapshot: recent conflicting therapies, unresolved safety findings, and protocol-prohibited concomitant conditions.

Site Locations

  • Site 46 University Hospital | PI: Dr. Kim | Closed
  • Site 206 Medical Center | PI: Dr. Patel | Closed
  • Site 366 Community Clinic | PI: Dr. Harper | Closed
  • Site 526 Medical Center | PI: Dr. Kim | Closed
  • Site 686 Community Clinic | PI: Dr. Harper | Closed
  • Site 846 Community Clinic | PI: Dr. Ruiz | Closed

Contact Study Team