A Study to Determine Safety, Tolerability, Pharmacokinetics, and Recommended Phase 2 Dose (RP2D) of Intravenous ABBV-184 in Adult Participants With Previously Treated Cancers

PHASE1TerminatedINTERVENTIONAL
Enrollment

14

Participants

Timeline

Start Date

May 5, 2020

Primary Completion Date

June 27, 2022

Study Completion Date

June 27, 2022

Conditions
Acute Myeloid Leukemia (AML)Non Small Cell Lung CancerCancer
Interventions
DRUG

ABBV-184

Intravenous (IV) infusion

Trial Locations (17)

33075

Hopital Saint-Andre /ID# 224218, Bordeaux

33604

CHU Bordeaux - Hopital Haut Leveque /ID# 224998, Pessac

44000

CHU de Nantes, Hotel Dieu -HME /ID# 215703, Nantes

44718

Gabrail Cancer Center Research /ID# 215667, Canton

46804

Fort Wayne Medical Oncology and Hematology, Inc /ID# 224332, Fort Wayne

59037

CHRU Lille - Hopital Claude Huriez /ID# 217508, Lille

3109601

Rambam Health Care Campus /ID# 215808, Haifa

5265601

The Chaim Sheba Medical Center /ID# 215810, Ramat Gan

6423906

Tel Aviv Sourasky Medical Center /ID# 222749, Tel Aviv

19107-4414

Thomas Jefferson University /ID# 218403, Philadelphia

06189

Centre Antoine Lacassagne - Nice /ID# 218014, Nice

464-8681

Aichi Cancer Center Hospital /ID# 216469, Nagoya

277-8577

National Cancer Center Hospital East /ID# 216467, Kashiwa-shi

104-0045

National Cancer Center Hospital /ID# 216466, Chuo-ku

OX3 9DU

Oxford University Hospitals NHS Foundation Trust /ID# 217252, Oxford

CF14 4XN

Cardiff & Vale University Health Board /ID# 217250, Cardiff

M20 4BX

The Christie Hospital /ID# 216118, Manchester

Sponsors

Lead Sponsor

All Listed Sponsors
lead

AbbVie

INDUSTRY