EMB-01 in Patients With Advanced/Metastatic Gastrointestinal Cancers
Study Details
Study Description
Brief Summary
This study is to evaluate the safety and antitumor activity of EMB-01 in advanced/metastatic gastrointestinal cancers, including gastric cancer, hepatocellular cancer, cholangiocarcinoma and colorectal cancer.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
| Phase 1/Phase 2 |
Detailed Description
This is an open-label, Phase Ib/II, multi-stage study of EMB-01 in patients with advanced gastrointestinal tumors including gastric cancer, hepatocellular cancer, cholangiocarcinoma cancer and colorectal cancer, who have EGFR/cMET gene alterations or protein over expression and progressed on available standard therapies and for whom no standard therapy exists that would confer clinical benefit. All patients will be prescreened for cMET and EGFR genetic alterations and protein expression. Only those who met the molecular pre-screening criteria will proceed to clinical screening to determine the eligibility. The study will consist of Phase Ib part and Phase II part, both phases will consist of a molecular prescreening period, screening period, treatment period, safety follow-up period, and disease progression follow-up.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Phase Ib and Phase II In phase 1b part of the study, the study will recruit approximate 6 patients to each of the 4 GI cancer groups (gastric cancer, hepatocellular cancer, cholangiocarcinoma and colorectal cancer) to characterize PK profile of EMB-01 at the RP2D (1600 mg QW) in GI cancers and evaluate the safety and tolerability of EMB-01 at the RP2D. In the Phase 2part of the study, additional patients will be enrolled into each of the 4 GI cancer groups (gastric cancer, hepatocellular cancer, cholangiocarcinoma, and colorectal cancer) until a total of 24 patients are treated at the RP2D. |
Drug: EMB-01
EMB-01 at the RP2D of 1600 mg will be administered as an IV infusion once weekly (QW) throughout the study. One cycle is defined as 4 weeks (4 doses). All patients will be premedicated with a histamine-1 (H1) receptor antagonist diphenhydramine (25 or 50 mg) intravenously 30-60 minutes prior to dosing in the first two cycles. Premedication for subsequent treatment cycles will depend on whether the patient develops infusion-related reactions (IRR), at the discretion of the investigator.
Other Names:
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Outcome Measures
Primary Outcome Measures
- Number of participants with Adverse Events and Serious Adverse Events as assessed by CTCAE v5.0 [Phase 1b, screening up to follow-up (30 days after the last dose)]
Number of participants with Adverse Events and Serious Adverse Events as assessed by CTCAE v5.0
- Best Overall Response (BOR) as assessed by RECIST v1.1 [Phase II, from the date of dosing until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 48 months]
Best Overall Response (BOR) as assessed by RECIST v1.1
- Objective Response Rate (ORR) as assessed by RECIST v1.1 [Phase II, from the date of dosing until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 48 months]
Objective Response Rate (ORR) as assessed by RECIST v1.1
- Duration of Response (DoR) as assess by RECIST v1.1 as assess by RECIST v1.1 [Phase II, from the date of dosing until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 48 months]
Duration of Response (DoR) as assess by RECIST v1.1 as assess by RECIST v1.1
- Disease Control Rate (DCR) as assess by RECIST v1.1 [Phase II, from the date of dosing until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 48 months]
Disease Control Rate (DCR) as assess by RECIST v1.1
- Progression-Free Survival (PFS) as assess by RECIST v1.1 [Phase II, from the date of dosing until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 48 months]
Progression-Free Survival (PFS) as assess by RECIST v1.1
- Maximum serum concentration (Cmax) of EMB-01 [Phase Ib only, up to 3 months after first study drug administration]
Maximum serum concentration (Cmax) of EMB-01
- Trough serum concentration (Ctrough) of EMB-01 [Phase Ib only, predose, through treatment completion, an average of 1 year]
Trough serum concentration (Ctrough) of EMB-01
- Area under the concentration-time curve from time 0 (pre-dose) to the time of the dosing interval (AUC0-t) [Phase Ib only, up to 3 months after first study drug administration]
Area under the concentration-time curve from time 0 (pre-dose) to the time of the dosing interval (AUC0-t)
- Area under the concentration-time curve from time 0 to infinity (AUC0-inf) [Phase Ib only, up to 3 months after first study drug administration]
Area under the concentration-time curve from time 0 to infinity (AUC0-inf)
- Elimination half-life (T1/2) [Phase Ib only, up to 3 months after first study drug administration]
Elimination half-life (T1/2)
- Systemic clearance (CL) [Phase Ib only, up to 3 months after first study drug administration]
Systemic clearance (CL)
- Apparent volume of distribution at steady-state (Vss) [Phase Ib only, up to 3 months after first study drug administration]
Apparent volume of distribution at steady-state (Vss)
- Accumulation Ratio (AR) after multiple dosing [Phase Ib only, up to 3 months after first study drug administration]
Accumulation Ratio (AR) after multiple dosing
- Incidence of positive ADA [Phase Ib only, up to the 30-day safety follow-up visit after EOT]
Incidence of positive ADA
Secondary Outcome Measures
- Number of participants with Adverse Events and Serious Adverse Events as assessed by CTCAE v5.0 [Phase II, screening up to follow-up (30 days after the last dose)]
Number of participants with Adverse Events and Serious Adverse Events as assessed by CTCAE v5.0
- Maximum serum concentration (Cmax) of EMB-01 [Phase II, up to 3 months after first study drug administration]
Maximum serum concentration (Cmax) of EMB-01
- Trough serum concentration (Ctrough) of EMB-01 [Phase II, predose, through treatment completion, an average of 1 year]
Trough serum concentration (Ctrough) of EMB-01
- Incidence of positive ADA [Phase II , up to the 30-day safety follow-up visit after EOT]
Incidence of positive ADA
- Best Overall Response (BOR) as assessed by RECIST v1.1 [Phase Ib, from the date of dosing until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 48 months]
Best Overall Response (BOR) as assessed by RECIST v1.1
- Objective Response Rate (ORR) as assessed by RECIST v1.1 [Phase Ib, from the date of dosing until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 48 months]
Objective Response Rate (ORR) as assessed by RECIST v1.1
- Duration of Response (DoR) as assess by RECIST v1.1 as assess by RECIST v1.1 [Phase Ib, from the date of dosing until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 48 months]
Duration of Response (DoR) as assess by RECIST v1.1 as assess by RECIST v1.1
- Disease Control Rate (DCR) as assess by RECIST v1.1 [Phase Ib, from the date of dosing until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 48 months]
Disease Control Rate (DCR) as assess by RECIST v1.1
- Progression-Free Survival (PFS) as assess by RECIST v1.1 [Phase Ib, from the date of dosing until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 48 months]
Progression-Free Survival (PFS) as assess by RECIST v1.1
Eligibility Criteria
Criteria
Inclusion Criteria:
Molecular Pre-screening Inclusion criteria (Phase II only)
-
cMET amplification in tumor sample: cMET gene copy number ≥5 or MET/CEP7 ratio ≥ 2 by FISH; OR
-
cMET overexpression in tumor sample: cMET expression ≥ 2+ by IHC, OR
-
EGFR overexpression in tumor sample: EGFR expression ≥ 3+ by IHC; OR
-
Other EGFR or cMET gene alteration in blood sample (circulating tumor DNA, ctDNA): point mutation causing activation of EGFR or cMET tyrosine kinase, insertion/deletion (indels), copy number amplification by NGS.
Screening Inclusion Criteria
-
Able to understand and willing to sign the Informed Consent Form (ICF).
-
Histologically/cytologically confirmed advanced/metastatic gastrointestinal cancer (including gastric cancer, hepatocellular cancer, cholangiocarcinoma and colorectal cancer) with measurable disease (RECIST V1.1). To be eligible, patients must meet following criteria:
-
Have failed all standard of care therapies known to confer clinical benefit. Patients who is not tolerable on standard of care therapies, or no standard of care therapies available, or refused standard of care therapies are eligible.
-
Have measurable disease as defined by RESIST v 1.1.
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Must have adequate organ function.
-
Regarding prior anti-tumor therapy:
-
Patients who have received any anticancer drugs approved or investigational, including chemotherapy, immune therapy, hormonal therapy (Exceptions: hormone-replacement therapy, testosterone or oral contraceptives), biologic therapy, must have stopped treatment at least 4 weeks or within 5 half -lives whichever shorter before first dose of EMB-01.
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Local radiotherapy or radiation therapy for bone metastases must have stopped 2 weeks before first dose of EMB-01. No therapeutic radiopharmaceuticals are taken within 8 weeks before first dose of EMB-01.
-
Patients who have received prior targeted therapies must have stopped treatment for at least 4 weeks or within 5 half-lives, whichever is shorter before first dose of EMB-01.
-
Female patient with fertility or male patient whose partner has fertility should use one or more contraceptive methods for contraception starting from screening period and continue throughout the study treatment and for 3 months.
-
ECOG score ≤2.
Exclusion Criteria:
Molecular Pre-screening Exclusion Criteria
Subject who meets any of the following criteria can't be proceeded to clinical screening:
-
Patients who are unwilling to sign the molecular pre-screening ICF.
-
Patients for whom the results of central laboratory testing do not meet the molecular pre-screening inclusion criteria.
Screening Exclusion Criteria
-
Life expectancy < 3 months.
-
Patients with primary central nervous system (CNS) malignancy or symptomatic CNS (leptomeningeal or brain) metastases are not allowed. Patients with asymptomatic CNS metastases are eligible.
-
Pregnant or nursing females.
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Patients who have had major surgery within the 28 days from the screening. Surgical wounds must be completely healed.
-
Any other serious underlying medical (e.g. uncontrolled diabetes mellitus, active uncontrolled infection, active gastric ulcer, uncontrolled seizures, cerebrovascular incidents, gastrointestinal bleeding, severe signs and symptoms of coagulation and clotting disorders, cardiac conditions), psychiatric, psychological, familial or geographical condition that, in the judgment of the investigator, may interfere with the planned staging, treatment and follow-up, affect patient compliance or place the patient at high risk from treatment-related complications.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Gabrail Cancer Center Research | Canton | Ohio | United States | 44718 |
| 2 | MD Anderson Cancer Center | Houston | Texas | United States | 77030 |
| 3 | Beijing cancer Hospital | Beijing | Beijing | China | 100142 |
| 4 | Nanfang Hospital | Guangzhou | Guangdong | China | 510515 |
Sponsors and Collaborators
- Shanghai EpimAb Biotherapeutics Co., Ltd.
- Labcorp Drug Development, Inc.
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- EMB01X201