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Clinical Trials/NCT04060342
NCT04060342
Terminated
Phase 1

A Phase 1/2, First-in-Human, Open-label, Dose Escalation Study of GB1275 Monotherapy and in Combination With an Anti-PD-1 Antibody in Patients With Specified Advanced Solid Tumors or in Combination With Standard of Care in Patients With Metastatic Pancreatic Adenocarcinoma, Followed by Basket Expansion of GB1275 With Standard of Care or in Combination With an Anti-PD-1 Antibody in Patients With Specified Metastatic Solid Tumors

GB006, Inc., a wholly owned subsidiary of Gossamer Bio, Inc.8 sites in 2 countries61 target enrollmentAugust 13, 2019

Overview

Phase
Phase 1
Intervention
GB1275
Conditions
Pancreatic Adenocarcinoma
Sponsor
GB006, Inc., a wholly owned subsidiary of Gossamer Bio, Inc.
Enrollment
61
Locations
8
Primary Endpoint
Phase 1 Dose Escalation - Regimens A, B,and C: Incidence of dose limiting toxicities (DLTs)
Status
Terminated
Last Updated
3 years ago

Overview

Brief Summary

This first-in-human (FIH ) study is an open-label, multicenter study that consists of a Phase 1 Dose Escalation/Expansion phase of GB1275 monotherapy or in combination with Anti-PD-1 Antibody or in combination with Standard of Care in Patients with Metastatic Pancreatic Adenocarcinoma followed by a Phase 2 Basket Expansion phase in Patients with Specified Metastatic Solid Tumors

Detailed Description

Note: The Phase 2 portion of the study was not initiated.

Registry
clinicaltrials.gov
Start Date
August 13, 2019
End Date
April 11, 2022
Last Updated
3 years ago
Study Type
Interventional
Study Design
Sequential
Sex
All

Investigators

Sponsor
GB006, Inc., a wholly owned subsidiary of Gossamer Bio, Inc.
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Subject has a performance status of 0 or 1 on the Eastern Cooperative Oncology Group (ECOG) Performance Scale.
  • Women of childbearing potential must use an acceptable method of contraception
  • Subjects with the the following:
  • Regimen A and B:
  • pancreatic adenocarcinoma,
  • esophageal adenocarcinoma, or esophageal squamous cell carcinoma, or
  • gastric/gastroesophageal junction adenocarcinoma, or
  • prostate cancer, or
  • colorectal adenocarcinoma, or subjects with tumor types that have progressed after receiving initial treatment benefit rom the last single agent checkpoint inhibitor that is approved for the indication or in combination with standard of care therapy, for example, non-small cell lung cancer, small cell lung cancer, head and neck squamous cell carcinoma, urothelial carcinoma, renal cell carcinoma, and hepatocellular carcinoma, etc.
  • Regimen C: newly diagnosed stage IV pancreatic cancer

Exclusion Criteria

  • History of another malignancy within 2 years prior to first study drug(s) administration, unless the malignancy was treated with curative intent and the likelihood of relapse is \<5% in 2 years
  • Pregnant or nursing
  • Known history of testing positive for human immunodeficiency virus (HIV)
  • Gastrointestinal (GI) tract disease causing the inability to take oral medication.
  • Positive test for Hepatitis B virus surface antigen (HBsAg) or a and/or positive Hep C antibody result with detectable hepatitis C virus (HCV) ribonucleic acid (RNA) indicating acute or chronic infection.
  • Other protocol-defined inclusion/exclusion criteria will apply

Arms & Interventions

Phase 1: Regimen A - GB1275 monotherapy

GB1275 Monotherapy dose escalation: Oral administration. Twice per day (BID).

Intervention: GB1275

Phase 1: Regimen B - GB1275 with an Anti-PD-1

GB1275 with pembrolizumab dose escalation and expansion: GB1275 oral administration; twice per day (BID), and pembrolizumab IV administration once every 3 weeks (Q3W).

Intervention: GB1275

Phase 1: Regimen B - GB1275 with an Anti-PD-1

GB1275 with pembrolizumab dose escalation and expansion: GB1275 oral administration; twice per day (BID), and pembrolizumab IV administration once every 3 weeks (Q3W).

Intervention: pembrolizumab

Phase 1: Regimen C - GB1275 with Standard of Care (SOC)

GB1275 with SOC dose escalation: GB1275 oral administration; twice per day (BID), and nab-paclitaxel and gemcitabine per United States Prescribing Information (USPI)

Intervention: GB1275

Phase 1: Regimen C - GB1275 with Standard of Care (SOC)

GB1275 with SOC dose escalation: GB1275 oral administration; twice per day (BID), and nab-paclitaxel and gemcitabine per United States Prescribing Information (USPI)

Intervention: nab-paclitaxel and gemcitabine

Phase 2: Cohort 1 - GB1275 with SOC

GB1275 with SOC Basket Cohort in patients with newly diagnosed metastatic pancreatic cancer: GB1275 oral administration; twice per day (BID) and nab-paclitaxel and gemcitabine per USPI.

Intervention: GB1275

Phase 2: Cohort 1 - GB1275 with SOC

GB1275 with SOC Basket Cohort in patients with newly diagnosed metastatic pancreatic cancer: GB1275 oral administration; twice per day (BID) and nab-paclitaxel and gemcitabine per USPI.

Intervention: nab-paclitaxel and gemcitabine

Phase 2: Cohort 2 - GB1275 with an Anti-PD-1

GB1275 with pembrolizumab Basket Cohort in patients with MSS colorectal cancer: GB1275 oral administration; twice per day (BID), and pembrolizumab IV administration once every 3 weeks (Q3W).

Intervention: GB1275

Phase 2: Cohort 2 - GB1275 with an Anti-PD-1

GB1275 with pembrolizumab Basket Cohort in patients with MSS colorectal cancer: GB1275 oral administration; twice per day (BID), and pembrolizumab IV administration once every 3 weeks (Q3W).

Intervention: pembrolizumab

Phase 2: Cohort 3 - GB1275 with an Anti-PD-1

GB1275 with pembrolizumab Basket Cohort in patients with gastric/GEJ cancer, PD-L1 positive: GB1275 oral administration; twice per day (BID), and pembrolizumab IV administration once every 3 weeks (Q3W).

Intervention: GB1275

Phase 2: Cohort 3 - GB1275 with an Anti-PD-1

GB1275 with pembrolizumab Basket Cohort in patients with gastric/GEJ cancer, PD-L1 positive: GB1275 oral administration; twice per day (BID), and pembrolizumab IV administration once every 3 weeks (Q3W).

Intervention: pembrolizumab

Outcomes

Primary Outcomes

Phase 1 Dose Escalation - Regimens A, B,and C: Incidence of dose limiting toxicities (DLTs)

Time Frame: Regimen A and B dose escalation Days 1-21, Regimen C dose escalation Days 8-36 days

Phase 1 Dose Escalation - Regimens A, B, and C and Phase 1 Expansion - Regimen B: Incidence of adverse events (AEs)

Time Frame: Regimen A and C from first dose through 30 days post last dose, Regimen B from first dose through 90 days post last dose

Phase 1 Dose Escalation - Regimens A and B: Cmax of GB1275

Time Frame: From first dose through 30 days post last dose

Maximum observed plasma concentration

Phase 1 Dose Escalation - Regimens A and B: Ctrough of GB1275

Time Frame: From first dose through 30 days post last dose

Trough observed plasma concentration

Phase 1 Dose Escalation - Regimens A and B: Tmax of GB1275

Time Frame: From first dose through 30 days post last dose

Time of maximum observed plasma concentration

Phase 1 Dose Escalation - Regimens A and B: AUC of GB1275

Time Frame: From first dose through 30 days post last dose

Area under the plasma concentration-time curve

Phase 1 Dose Escalation - Regimens A and B: t1/2 of GB1275

Time Frame: From first dose through 30 days post last dose

Terminal phase elimination half-life

Phase 1 Dose Escalation - Regimens A and B: CL/F of GB1275

Time Frame: From first dose through 30 days post last dose

Oral clearance

Phase 2 - Basket Cohorts 1, 2 and 3: Objective Response Rate (ORR)

Time Frame: 24 months

ORR defined as the proportion of subjects with best overall confirmed response (BOCR) of either a complete response (CR) or partial response (PR) as assessed by the Investigator based on RECIST v1.1

Secondary Outcomes

  • Phase 1 - Regimen C and Phase 1 Expansion - Regimen B: t1/2 of GB1275(From first dose through 30 days post last dose)
  • Phase 1 - Regimen C and Phase 1 Expansion - Regimen B: AUC of GB1275(From first dose through 30 days post last dose)
  • Phase 1 - Regimen C and Phase 1 Expansion - Regimen B: CL/F of GB1275(From first dose through 30 days post last dose)
  • Phase 1 - Regimen C: Cmax of nab-paclitaxel and gemcitabine(From first dose through 30 days post last dose)
  • Phase 1 - Regimen C: Tmax of nab-paclitaxel and gemcitabine)(From first dose through 30 days post last dose)
  • Phase 1 - Regimen C: AUC of nab-paclitaxel and gemcitabine(From first dose through 30 days post last dose)
  • Phase 2 - Basket Cohorts 1, 2, and 3: Duration of Response (DOR)(24 months)
  • Phase 2 - Basket Cohorts 1, 2, and 3: Time to Response (TTR)(24 months)
  • Phase 1 - Regimen C and Phase 1 Expansion - Regimen B: Cmax of GB1275(From first dose through 30 days post last dose)
  • Phase 1 - Regimen C and Phase 1 Expansion - Regimen B: Ctrough of GB1275(From first dose through 30 days post last dose)
  • Phase 1 - Regimen C and Phase 1 Expansion - Regimen B: Tmax of GB1275(From first dose through 30 days post last dose)
  • Phase 2 - Basket Cohorts 1, 2, and 3: Clinical Benefit Rate (CBR)(6 months)
  • Phase 2 - Basket Cohorts 1, 2, and 3: Progression Free Survival (PFS)(24 months)
  • Phase 2 - Basket Cohorts 1, 2, and 3: Time to Progression (TTP)(24 months)
  • Phase 2 - Basket Cohorts 1, 2, and 3: Overall Survival (OS)(24 months)
  • Phase 2 - Basket Cohorts 1, 2, and 3: Incidence of AEs(Basket Cohorts 1 from first dose through 30 days post last dose, Basket Cohorts 2 and 3 from first dose through 90 days post last dose.)
  • Phase 2 - Basket Cohort 1, 2 and 3: PK profile of GB1275(Basket Cohorts 1, 2, and 3 from first dose through 30 days post last dose.)

Study Sites (8)

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