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BRIEF TITLE: Study to Determine the Safety, Tolerability, Pharmacokinetics and RP2D of ABBV-151 as a Single Agent and in Combination With ABBV-181 in Subjects With Locally Advanced or Metastatic Solid Tumors

A Phase 1 First-in Human, Multi-Center, Open Label Dose-Escalation Study to Determine the Safety, Tolerability, Pharmacokinetics and RP2D of ABBV-151 as a Single Agent and in Combination With ABBV-181 in Subjects With Locally Advanced or Metastatic Solid Tumors


  • Org Study ID: M19-345
  • Secondary ID: 2018-004303-40
  • NCT ID: NCT03821935
  • NCT Alias:
  • Sponsor: AbbVie - Industry
  • Source: AbbVie

Brief Summary

The study will determine the recommended Phase 2 dose (RP2D) of ABBV-151 administered as monotherapy and in combination with ABBV-181 as well as to assess the safety, pharmacokinetics (PK), and preliminary efficacy of ABBV-151 alone and in combination with ABBV-181. The study will consist of 2 phases: dose escalation and dose expansion.

Overal Status Start Date Phase Study Type
Recruiting February 21, 2019 Phase 1 Interventional

Primary Outcomes:

Primary Outcome 1 - Measure: Dose Escalation: Recommended Phase 2 Dose (RP2D) ABBV-151 Monotherapy

Primary Outcome 1 - Time Frame: Up to 28 days after the first dose of ABBV-151 monotherapy

Primary Outcome 2 - Measure: Dose Escalation: RP2D ABBV-151 + ABBV-181 Combination Therapy

Primary Outcome 2 - Time Frame: Up to 28 days after the first dose of ABBV-151 and ABBV-181 combination therapy

Primary Outcome 3 - Measure: Dose Expansion: Objective Response Rate (ORR)

Primary Outcome 3 - Time Frame: Up to approximately 6 months after the first dose date of last participant in Dose Expansion

Condition:

  • Advanced Solid Tumors Cancer

Eligibility

Criteria:
Inclusion Criteria:

- For Dose Escalation only: Participants with an advanced solid tumor who are considered
refractory to or intolerant of all existing therapy(ies) known to provide a clinical
benefit for their condition. Additionally, participants who have been offered standard
therapies and refused, or who are considered ineligible for standard therapies, may be
eligible for this study on a case-by-case basis, after discussion with and agreement
from the sponsor. Participants with triple-negative breast cancer (TNBC), pancreatic
adenocarcinoma, urothelial cancer, Hepatocellular carcinoma (HCC), or Head and neck
squamous cell carcinoma (HNSCC) who are being considered for the dose escalation
cohorts must also meet the histology specific eligibility criteria described below for
dose expansion

- For Dose Expansion only participants must meet criteria specific to the type of
cancer:

- TNBC - Female or male participants with confirmed breast adenocarcinoma that is
ER-negative, PR-negative, and HER2-negative, (as defined per American Society of
Clinical Oncology [ASCO]/College of American Pathology [CAP] guidelines), who must
have disease progression during or after at least 1 systemic therapy that included a
taxane in the metastatic or recurrent setting.

- Pancreatic adenocarcinoma and have disease progression during or after 1 systemic
therapy (gemcitabine monotherapy or in combination with other agents, FOLFIRINOX [or
another regimen including both 5-fluorouracil and oxaliplatin], capecitabine
monotherapy or in combination with other agents) administered in the adjuvant, locally
advanced, or metastatic setting. If the therapy was used in an adjuvant setting,
disease progression must have occurred within 6 months of completing adjuvant therapy.

- Urothelial cancer of the bladder and urinary tract and must have progressed following
treatment with a platinum-based regimen (administered in any line of therapy) and a
programmed death 1/programmed death ligand 1 (PD1/PDL1) antagonist administered in the
recurrent or metastatic setting (progression following a PD1/PDL1 antagonist is
defined as unequivocal progression on or within 3 months of the last dose of anti-PD1
or anti-PDL1 therapy).

- HCC and must have disease progression during or after 1 prior line of systemic
therapy.

- HNSCC (arising from the oral cavity, oropharynx, hypopharynx, or larynx) and must have
progressed following treatment with platinum-based regimen (administered in any line
of therapy) and a PD1/PDL1 antagonist administered in the recurrent or metastatic
setting (progression following a PD1/PDL1 antagonist is defined as unequivocal
progression on or within 3 months of the last dose of anti-PD1 or anti-PDL1 therapy).

- Participant has an Eastern Cooperative Oncology Group (ECOG) Performance Status of 0
to 1.

- Participant has adequate bone marrow, renal, hepatic, and coagulation function. Must
have a viral status consistent with the requirements described in the protocol
specific to type of cancer and stage of study (Dose Escalation or Dose Expansion).

Exclusion Criteria:

- For Dose Expansion only: Participants (except for participants with urothelial cancer
or HNSCC) who have had prior exposure to immunotherapies as listed in the protocol.

- Has received anticancer therapy including chemotherapy, immunotherapy, radiation
therapy, biologic, herbal therapy, or any investigational therapy within a period of 5
half-lives or 28 days (whichever is shorter), prior to the first dose of the study
drug.

- Participant has unresolved AEs > Grade 1 from prior anticancer therapy except for
alopecia.

- Has a history of primary immunodeficiency, bone marrow transplantation, solid organ
transplantation, or previous clinical diagnosis of tuberculosis.

- Has a known uncontrolled metastases to the central nervous system (with certain
exceptions).

- Current or prior use of immunosuppressive medication within 14 days prior to the first
dose of the study drug.
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Gender: All

Minimum Age: 18 Years

Maximum Age: N/A

Healthy Volunteers: No

Official Information

Name: AbbVie Inc.

Role: Study Director

Affiliation: AbbVie

Overall Contact

Name: ABBVIE CALL CENTER

Phone: 847.283.8955

Email: abbvieclinicaltrials@abbvie.com

Locations

Facility Status Contact
Yale University /ID# 208356
New Haven, Connecticut 06510
United States
Recruiting
Indiana Univ School Medicine /ID# 208384
Indianapolis, Indiana 46202
United States
Recruiting
Univ Michigan Med Ctr /ID# 221129
Ann Arbor, Michigan 48109
United States
Not yet recruiting
NYU Langone Medical Center /ID# 209822
New York, New York 10016-6402
United States
Not yet recruiting
Carolina BioOncology Institute /ID# 208358
Huntersville, North Carolina 28078
United States
Recruiting
The Ohio State University - The James /ID# 217611
Columbus, Ohio 43210-1240
United States
Not yet recruiting
NEXT Oncology /ID# 208930
San Antonio, Texas 78229
United States
Recruiting
Chris O'Brien Lifehouse /ID# 213236
Camperdown, New South Wales 2050
Australia
Recruiting
Princess Margaret Cancer Centre /ID# 209423
Toronto, Ontario M5G 2M9
Canada
Recruiting
Hopital Universitaire Purpan /ID# 218667
Toulouse, Haute-Garonne 31059
France
Not yet recruiting
Centre Leon Berard /ID# 218515
Lyon CEDEX 08, Rhone 69373
France
Not yet recruiting
Institut Gustave Roussy /ID# 218668
Villejuif, Val-de-Marne 94800
France
Not yet recruiting
Rambam Health Care Campus /ID# 222198
Haifa, 3109601
Israel
Not yet recruiting
Sheba Medical Center /ID# 209037
Ramat Gan, 5262100
Israel
Recruiting
Tel Aviv Sourasky Medical Center /ID# 222199
Tel Aviv-Yafo, 6423906
Israel
Not yet recruiting
National Cancer Center Hospital /ID# 209421
Chuo-ku, Tokyo 104-0045
Japan
Recruiting
Seoul National University Hospital /ID# 218513
Seoul, 03080
Korea, Republic of
Not yet recruiting
Severance Hospital /ID# 218512
Seoul, 03722
Korea, Republic of
Not yet recruiting
Hospital Clinic de Barcelona /ID# 221106
Barcelona, 08036
Spain
Not yet recruiting
Hospital Fundacion Jimenez Dia /ID# 220928
Madrid, 28040
Spain
Not yet recruiting
Hosp Clin Univ de Valencia /ID# 221107
València, 46010
Spain
Not yet recruiting
China Medical University Hosp /ID# 218492
Taichung City, Taichung 40447
Taiwan
Not yet recruiting
National Taiwan University Hospital /ID# 218490
Taipei City, Taipei 100
Taiwan
Not yet recruiting