# Efficacy and Safety of Oral HBI-8000 in Patients With Relapsed or Refractory Adult T Cell Lymphoma (ATL)

> **NCT02955589** · PHASE2 · COMPLETED · sponsor: **HUYABIO International, LLC.** · enrollment: 23 (actual)

## Conditions studied

- Adult T-Cell Lymphoma (ATL)

## Interventions

- **DRUG:** HBI-8000

## Key facts

- **NCT ID:** NCT02955589
- **Lead sponsor:** HUYABIO International, LLC.
- **Sponsor class:** INDUSTRY
- **Phase:** PHASE2
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2016-11
- **Primary completion:** 2018-12
- **Final completion:** 2019-11
- **Target enrollment:** 23 (ACTUAL)
- **Last updated:** 2024-09-19

## Collaborators

- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT02955589

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT02955589, "Efficacy and Safety of Oral HBI-8000 in Patients With Relapsed or Refractory Adult T Cell Lymphoma (ATL)". Retrieved via AI Analytics 2026-08-01 from https://api.ai-analytics.org/clinical/NCT02955589. Licensed CC0.

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