AB122 Platform Study

⚠️

This is not medical advice. AI-assisted translation — inaccuracies may occur. Always verify the original and consult your oncologist before taking any steps.

About the trial

This is a phase 1, non-randomized open-label, multicenter platform study designed to evaluate the tolerability and safety of AB122 in patients with malignancies specified in each cohort.

Original English text from ClinicalTrials.gov

Who can (and can't) join

✓ Qualifies

  • Wiek co najmniej 18 lat
  • Zdolność do uczestniczenia w badaniu i przychodzenia na wizyty
  • Dobry ogólny stan zdrowia (ECOG 0-1)
  • Prawidłowa funkcja wątroby i nerek
  • Wystarczająca liczba białych krwinek (minimum 1500/mm3)
  • Wystarczająca liczba płytek krwi (minimum 100000/mm3)
  • Hemoglobina co najmniej 9,0 g/dL
  • Spodziewana długość życia co najmniej 90 dni

Simplified criteria — AI translation

Trial details

Minimum age
18 Years
Last updated (source)
August 5, 2026
Sex
No restrictions

Therapies / drugs in trial

Locations (9)

A site selected by Taiho Pharmaceutical Co., Ltd.

Aichi, Japan

A site selected by Taiho Pharmaceutical Co., Ltd.

Chiba, Japan

A site selected by Taiho Pharmaceutical Co., Ltd.

Ehime, Japan

A site selected by Taiho Pharmaceutical Co., Ltd.

Hokkaido, Japan

A site selected by Taiho Pharmaceutical Co., Ltd.

Kanagawa, Japan

A site selected by Taiho Pharmaceutical Co., Ltd.

Osaka, Japan

A site selected by Taiho Pharmaceutical Co., Ltd.

Shizuoka, Japan

A site selected by Taiho Pharmaceutical Co., Ltd.

Tokyo, Japan

A site selected by Taiho Pharmaceutical Co., Ltd.

Wakayama, Japan

Trial contact

Contact information from ClinicalTrials.gov. Contact in English.

Share this trial

Data from ClinicalTrials.gov. AI-assisted translation, last sync: 8/6/2026.

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