A Phase 2, Randomized Study to Evaluate Safety, Efficacy, and Optimal Dose of ABBV-400 in Combination With Fluorouracil, Folinic Acid, and Bevacizumab and to Evaluate Safety and Efficacy of ABBV-400 in Combination With Bevacizumab in Previously Treated Subjects With Unresectable Metastatic Colorectal Cancer

Status: Recruiting
Location: See all (64) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

Cancer is a condition where cells in a specific part of body grow and reproduce uncontrollably. The purpose of this study is to assess adverse events and change in disease activity when ABBV-400 is given in combination with Fluorouracil, Folinic Acid, and Bevacizumab to adult participants to treat unresctable metastatic colorectal cancer. ABBV-400 is an investigational drug being developed for the treatment of unresectable metastatic colorectal cancer. Fluorouracil, folinic acid, and bevacizumab (FFB) is an approved drug for the treatment of unresectable metastatic colorectal cancer. Study doctors put the participants in groups called treatment arms. Each treatment arm receives a different dose of ABBV-400 in combination with FFB in escalating doses on two different schedules (safety lead in), followed by low or high doses of ABBV-400 in combination with FFB or fluorouracil, folinic acid, irinotecan, and bevacizumab (standard of care \[SOC\]) \[dose optimization\] on its own, ending with low or high doses of ABBV-400 in combination with FFB for continued dose optimization and expansion. Approximately 280 adult participants with unresectable metastatic colorectal cancer will be enrolled in the study in 65 sites worldwide. In the safety lead in, participants will receive escalating intravenous (IV) ABBV-400 in combination with IV FFB on two different schedules. During the dose optimization participants will receive IV ABBV-400 in combination with IV FFB at low or high doses determined in the safety lead in. The dose optimization arm will also include a comparator cohort in which participants will receive SOC. During the dose optimization and expansion stage, participants will receive IV ABBV-400 in combination with IV FFB at low or high doses that have been determined from the previous stages. The study will run for a duration of approximately 3 years. There may be higher treatment burden for participants in this trial compared to their standard of care. Participants will attend regular visits during the study at an approved institution (hospital or clinic). The effect of the treatment will be frequently checked by medical assessments, blood tests, questionnaires and side effects.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Diagnosis of histologically or cytologically confirmed unresectable metastatic colorectal cancer (mCRC).

• Measurable disease per Response Evaluation Criteria in Solid Tumors (RECIST) v1.1.

• Progressed on only one first-line (1L) systemic treatment of combination chemotherapy in the metastatic setting with or without targeted therapy.

Locations
United States
Arkansas
Highlands Oncology Group, PA /ID# 259424
COMPLETED
Springdale
Arizona
Mayo Clinic Arizona /ID# 262610
RECRUITING
Phoenix
California
City of Hope National Medical Center /ID# 257576
RECRUITING
Duarte
City of Hope - Orange County Lennar Foundation Cancer Center /ID# 268365
RECRUITING
Irvine
Connecticut
Yale School of Medicine /ID# 257494
RECRUITING
New Haven
Florida
Mayo Clinic Hospital Jacksonville /ID# 262609
RECRUITING
Jacksonville
Illinois
Northwestern Medicine - Northwestern Memorial Hospital /ID# 260563
RECRUITING
Chicago
University of Illinois Hospital and Health Sciences System /ID# 257300
RECRUITING
Chicago
Indiana
Fort Wayne Medical Oncology and Hematology- South Office /ID# 259601
RECRUITING
Fort Wayne
Community Health Network, Inc. /ID# 257078
RECRUITING
Indianapolis
Indiana University Melvin and Bren Simon Cancer Center /ID# 258789
RECRUITING
Indianapolis
Louisiana
Comprehensive Cancer Centers of Nevada /ID# 257642
RECRUITING
Henderson
Minnesota
Mayo Clinic - Rochester /ID# 257301
RECRUITING
Rochester
North Carolina
Levine Cancer Institute /ID# 258840
RECRUITING
Charlotte
Duke Cancer Center /ID# 257236
RECRUITING
Durham
Oregon
Oregon Health & Science University, Knight Cancer Institute- /ID# 259190
RECRUITING
Portland
South Carolina
Medical University of South Carolina /ID# 258486
RECRUITING
Charleston
South Dakota
Avera Cancer Institute /ID# 257949
RECRUITING
Sioux Falls
Texas
MD Anderson Cancer Center /ID# 258713
RECRUITING
Houston
Texas Oncology PA /ID# 257780
RECRUITING
Houston
Virginia
Inova Schar Cancer Institute - Fairfax - Innovation Park Drive /ID# 257448
RECRUITING
Fairfax
Virginia Cancer Specialists - Fairfax /ID# 257261
RECRUITING
Fairfax
Other Locations
Belgium
Institut Jules Bordet /ID# 257625
RECRUITING
Anderlecht
Imelda Ziekenhuis /ID# 257082
RECRUITING
Bonheiden
Cliniques Universitaires UCL Saint-Luc /ID# 257081
RECRUITING
Brussels
Universitair Ziekenhuis Antwerpen /ID# 257080
RECRUITING
Edegem
UZ Gent /ID# 257083
RECRUITING
Ghent
Universitair Ziekenhuis Leuven /ID# 257079
RECRUITING
Leuven
AZ-Delta /ID# 257084
RECRUITING
Roeselare
Germany
Charite Universitaetsmedizin Berlin Campus Virchow-Klinikum /ID# 257785
RECRUITING
Berlin
Universitaetsklinikum Carl Gustav Carus Dresden /ID# 257787
RECRUITING
Dresden
Universitaetsklinikum Hamburg-Eppendorf /ID# 257782
RECRUITING
Hamburg
Universitatsklinikum Mannheim /ID# 257781
RECRUITING
Mannheim
Universitaetsklinikum Tuebingen /ID# 258780
RECRUITING
Tübingen
Universitaetsklinikum Ulm /ID# 257783
RECRUITING
Ulm
Israel
Rambam Health Care Campus /ID# 257344
RECRUITING
Haifa
Hadassah /ID# 257088
RECRUITING
Jerusalem
Shaare Zedek Medical Center /ID# 259253
RECRUITING
Jerusalem
Meir Medical Center /ID# 257089
RECRUITING
Kfar Saba
The Chaim Sheba Medical Center /ID# 257312
RECRUITING
Ramat Gan
Assuta Medical Center /ID# 267581
RECRUITING
Tel Aviv
Tel Aviv Sourasky Medical Center /ID# 257090
RECRUITING
Tel Aviv
Japan
National Cancer Center Hospital /ID# 257284
RECRUITING
Chuo-ku
National Cancer Center Hospital East /ID# 257282
RECRUITING
Kashiwa-shi
Kyoto University Hospital /ID# 257287
RECRUITING
Kyoto
Aichi Cancer Center Hospital /ID# 257286
RECRUITING
Nagoya
Shizuoka Cancer Center /ID# 257288
RECRUITING
Sunto-gun
Republic of Korea
Chonnam National University Hwasun Hospital /ID# 258366
RECRUITING
Hwasun-gun
Asan Medical Center /ID# 257845
RECRUITING
Seoul
Samsung Medical Center /ID# 257571
RECRUITING
Seoul
Seoul National University Hospital /ID# 257493
RECRUITING
Seoul
Yonsei University Health System Severance Hospital /ID# 257492
RECRUITING
Seoul
Spain
Hospital Universitario Vall de Hebron /ID# 257383
RECRUITING
Barcelona
Hospital General Universitario Gregorio Maranon /ID# 257387
RECRUITING
Madrid
Hospital Universitario 12 de Octubre /ID# 257384
RECRUITING
Madrid
Hospital Universitario HM Sanchinarro /ID# 258549
RECRUITING
Madrid
Hospital Clinico Universitario de Valencia /ID# 257385
RECRUITING
Valencia
Hospital Universitario Miguel Servet /ID# 257388
RECRUITING
Zaragoza
Taiwan
Kaohsiung Chang Gung Memorial Hospital /ID# 257675
RECRUITING
Kaohsiung City
Kaohsiung Medical University Chung-Ho Memorial Hospital /ID# 257637
RECRUITING
Kaohsiung City
National Cheng Kung University Hospital /ID# 257638
RECRUITING
Tainan City
Taipei Veterans General Hosp /ID# 257636
RECRUITING
Taipei
National Taiwan University Hospital /ID# 257639
RECRUITING
Taipei City
Linkou Chang Gung Memorial Hospital /ID# 257640
RECRUITING
Taoyuan
Contact Information
Primary
ABBVIE CALL CENTER
abbvieclinicaltrials@abbvie.com
844-663-3742
Time Frame
Start Date: 2023-11-12
Estimated Completion Date: 2026-10
Participants
Target number of participants: 280
Treatments
Experimental: Stage 1: ABBV-400+FFB A
Participants will receive escalating ABBV-400 in combination with Fluorouracil, Folinic Acid, and Bevacizumab (FFB) on dose schedule A as part of the safety lead in, during the 3 year study duration.
Experimental: Stage 1: ABBV-400+FFB B
Participants will receive escalating ABBV-400 in combination with FFB on dose schedule B as part of the safety lead in, during the 3 year study duration.
Experimental: Stage 2: ABBV-400+FFB A Low
Participants will receive ABBV-400 in combination with FFB at the low dose determined in the safety lead in on dose schedule A as part of the dose optimization, during the 3 year study duration.
Experimental: Stage 2: ABBV-400+FFB A High
Participants will receive ABBV-400 in combination with FFB at the high dose determined in the safety lead in on dose schedule A as part of the dose optimization, during the 3 year study duration.
Experimental: Stage 2: FFB+Irinotecan (Standard of Care [SOC])
Participants will receive SOC during the 3 year study duration.
Experimental: Stage 3: ABBV-400+FFB B Low
Participants will receive ABBV-400 in combination with FFB at the low dose determined in the safety lead in on dose schedule A as part of the dose optimization/expansion, during the 3 year study duration.
Experimental: Stage 3: ABBV-400+Bevacizumab C High
Participants will receive ABBV-400 in combination with Bevacizumab at the high dose determined in the safety lead in on dose schedule C as part of the dose optimization/expansion, during the 3 year study duration.
Related Therapeutic Areas
Sponsors
Leads: AbbVie

This content was sourced from clinicaltrials.gov

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