Clinical Trials /

DS-1205c With Osimertinib for Metastatic or Unresectable Epidermal Growth Factor Receptor (EGFR)-Mutant Non-Small Cell Lung Cancer

NCT03255083

Description:

This study has two parts: dose escalation and dose expansion. The primary objectives are: - For Dose Escalation, to assess the safety and tolerability of DS-1205c when combined with osimertinib in the study population and to determine the recommended dose for expansion of DS-1205c when combined with osimertinib in the study population - For Dose Expansion, to assess the safety and tolerability of DS-1205c when combined with osimertinib in the study population In Dose Escalation, after a 7-day run in period (Cycle 0), there will be 21-day cycles (Cycle 1 onward). In Dose Expansion, there will be 21-day cycles. The number of treatment cycles is not fixed in this study. Participants will continue study treatment for 36 months unless they decide not to (withdraw consent), their disease gets worse [progressive disease (PD)], or side effects become unacceptable (unacceptable toxicity).

Related Conditions:
  • Non-Small Cell Lung Carcinoma
Recruiting Status:

Recruiting

Phase:

Phase 1

Trial Eligibility

Document

Title

  • Brief Title: DS-1205c With Osimertinib for Metastatic or Unresectable Epidermal Growth Factor Receptor (EGFR)-Mutant Non-Small Cell Lung Cancer
  • Official Title: A Multicenter, Open-Label Phase 1 Study of DS-1205c in Combination With Osimertinib in Subjects With Metastatic or Unresectable EGFR-Mutant Non-Small Cell Lung Cancer

Clinical Trial IDs

  • ORG STUDY ID: DS1205-A-U101
  • SECONDARY ID: 2017-000542-21
  • NCT ID: NCT03255083

Conditions

  • Non-small Cell Lung Cancer (NSCLC)

Interventions

DrugSynonymsArms
DS-1205cDS-1205c with osimertinib
OsimertinibDS-1205c with osimertinib

Purpose

This study has two parts: dose escalation and dose expansion. The primary objectives are: - For Dose Escalation, to assess the safety and tolerability of DS-1205c when combined with osimertinib in the study population and to determine the recommended dose for expansion of DS-1205c when combined with osimertinib in the study population - For Dose Expansion, to assess the safety and tolerability of DS-1205c when combined with osimertinib in the study population In Dose Escalation, after a 7-day run in period (Cycle 0), there will be 21-day cycles (Cycle 1 onward). In Dose Expansion, there will be 21-day cycles. The number of treatment cycles is not fixed in this study. Participants will continue study treatment for 36 months unless they decide not to (withdraw consent), their disease gets worse [progressive disease (PD)], or side effects become unacceptable (unacceptable toxicity).

Trial Arms

NameTypeDescriptionInterventions
DS-1205c with osimertinibExperimentalParticipants receive DS-1205c (at planned doses given orally twice daily: 200 mg, 400 mg, 600 mg, 800 mg) in combination with daily 80 mg oral dose of osimertinib
  • DS-1205c
  • Osimertinib

Eligibility Criteria

        Inclusion Criteria:

          1. Has histologically or cytologically documented adenocarcinoma NSCLC.

          2. Has locally advanced or metastatic NSCLC, not amenable to curative surgery or
             radiation.

          3. Has acquired resistance to EGFR TKI according to the Jackman criteria (PMID:
             19949011):

               1. Historical confirmation that the tumor harbors an EGFR mutation known to be
                  associated with EGFR TKI sensitivity (including G719X, exon 19 deletion, L858R,
                  L861Q).

               2. Has experienced clinical benefit from an EGFR TKI, followed by systemic
                  progression (Response Evaluation Criteria in Solid Tumors [RECIST version 1.1] or
                  World Health Organization [WHO]) while on continuous treatment with an EGFR TKI.

          4. Is currently receiving and able to discontinue erlotinib, gefinitib, or afatinib.

          5. Has been receiving erlotinib, gefitinib, or afatinib for at least 6 weeks with
             well-controlled related toxicities less than Grade 3 in severity at the time of
             screening period.

          6. Has radiological documentation of disease progression while receiving continuous
             treatment with erlotinib, gefitinib, or afatinib.

          7. Has at least one measurable lesion per RECIST version 1.1.

          8. Is willing to provide archival tumor tissue from a biopsy performed within 6 months of
             progression during treatment with erlotinib, gefitinib, or afatinib OR has at least
             one lesion, not previously irradiated, amenable to core biopsy and is willing to
             undergo screening tumor biopsy.

          9. Demonstrates absence of EGFR T790M.

         10. Has Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1, with no
             deterioration over the previous 2 weeks.

        Exclusion Criteria:

          1. Has any evidence of small cell histology, or combined small cell and non-small cell
             histology, in original tumor biopsy or in screening biopsy performed since
             progression.

          2. Has previously documented evidence of ALK fusion, ROS1 fusion, BRAF V600E mutation,
             RET rearrangement, HER2 mutation, MET amplification, or MET exon 14 skipping mutation.
             No new testing for these genomic alterations is required for Screening.

          3. Has received treatment with any of the following:

               1. Any cytotoxic chemotherapy, immune checkpoint inhibitor therapy, investigational
                  agent or other anticancer drug(s) from a previous cancer treatment regimen or
                  clinical study (other than EGFR TKI), within 14 days of the first dose of study
                  treatment.

               2. Immune checkpoint inhibitor therapy within 30 days of first dose of study
                  treatment.

               3. Major surgery (excluding placement of vascular access) within 4 weeks of the
                  first dose of study treatment.

               4. Radiotherapy treatment to more than 30% of the bone marrow or with a wide field
                  of radiation within 4 weeks, or palliative radiation therapy within 2 weeks of
                  the first dose of study drug treatment.

          4. Has history of other active malignancy within 3 years prior to enrollment, except:

               1. Adequately treated non-melanoma skin cancer OR

               2. Superficial bladder tumors (Ta, Tis, T1) OR

               3. Curatively treated in situ disease

          5. Has spinal cord compression or clinically active brain metastases, defined as
             untreated and symptomatic, or requiring therapy with corticosteroids or
             anticonvulsants to control associated symptoms. Subjects with clinically inactive
             brain metastases may be included in the study. Subjects with treated brain metastases
             that are no longer symptomatic and who require no treatment with corticosteroids or
             anticonvulsants may be included in the study if they have recovered from the acute
             toxic effect of radiotherapy. A minimum of 2 weeks must have elapsed between the end
             of whole brain radiotherapy and study enrollment (1 week for stereotactic
             radiotherapy).

          6. Presence of retinal disease in the eye that is not due to neovascular age-related
             macular degeneration (nAMD; eg, significant diabetic retinopathy, glaucomatous retinal
             atrophy, retinal detachment).

          7. Has history of myocardial infarction within the past 6 months.

          8. Has symptomatic congestive heart failure (New York Heart Association [NYHA] Classes
             II-IV), unstable angina, or cardiac arrhythmia requiring antiarrhythmic treatment.

          9. Has left ventricular ejection fraction (LVEF) < 45% by either echocardiogram (ECHO) or
             multigated acquisition (MUGA) scan.

         10. Has any clinically important abnormalities in rhythm, conduction or morphology of
             resting ECG, eg, complete left bundle branch block, third-degree heart block,
             second-degree heart block, or PR interval > 250 milliseconds (ms).

         11. Has a mean QTcF prolongation >470 ms for females and >450 ms for males in three
             successive Screening measurements.

         12. Unable or unwilling to discontinue concomitant use of drugs that are known to prolong
             the QT interval.

         13. Has any factors that increase the risk of QTc prolongation or risk of arrhythmic
             events, such as congenital long QT. syndrome, family history of long QT syndrome or
             unexplained sudden death under 40 years of age in first degree relatives.

         14. Has any history of interstitial lung disease (pulmonary fibrosis or severe radiation
             pneumonitis) or is suspected to have such disease by imaging during screening.
      
Maximum Eligible Age:N/A
Minimum Eligible Age:18 Years
Eligible Gender:All
Healthy Volunteers:No

Primary Outcome Measures

Measure:Number of participants with dose-limiting toxicities (DLTs) during the Dose Escalation period
Time Frame:within 28 days
Safety Issue:
Description:An adverse event (AE) is any unfavorable and unintended sign (including an abnormal laboratory finding, for example), symptom, or disease temporally associated with the use of a medicinal product, whether or not considered related to the medicinal product.

Secondary Outcome Measures

Measure:Plasma concentration of DS-1205a versus time
Time Frame:during the 7 day run-in period
Safety Issue:
Description:
Measure:Maximum observed analyte concentration (Cmax)
Time Frame:during the 7 day run-in period
Safety Issue:
Description:
Measure:Actual sampling time to reach Cmax (Tmax)
Time Frame:during the 7 day run-in period
Safety Issue:
Description:
Measure:Area under the analyte concentration versus time curve during a dosing interval (AUCtau)
Time Frame:during the 7 day run-in period
Safety Issue:
Description:
Measure:Minimum observed analyte concentration prior to the beginning, or at the end, of a dosing interval (Ctrough)
Time Frame:during the 7 day run-in period
Safety Issue:
Description:
Measure:Cmax during a dosing interval (Tau) at steady state (Cmax,ss)
Time Frame:during the dose expansion period, within 36 months
Safety Issue:
Description:Categories: DS-1205a, osimertinib, and osimertinib active metabolites (AZ5104 and AZ7550)
Measure:Plasma concentration of DS-1205a versus time
Time Frame:during the dose expansion period, within 36 months
Safety Issue:
Description:Categories: DS-1205a, osimertinib, and osimertinib active metabolites (AZ5104 and AZ7550)
Measure:Tmax
Time Frame:during the dose expansion period, within 36 months
Safety Issue:
Description:Categories: DS-1205a, osimertinib, and osimertinib active metabolites (AZ5104 and AZ7550)
Measure:Ctrough
Time Frame:during the dose expansion period, within 36 months
Safety Issue:
Description:Categories: DS-1205a, osimertinib, and osimertinib active metabolites (AZ5104 and AZ7550)
Measure:AUCtau
Time Frame:during the dose expansion period, within 36 months
Safety Issue:
Description:Categories: DS-1205a, osimertinib, and osimertinib active metabolites
Measure:Objective response rate (ORR), graded according to RECIST version 1.1
Time Frame:within 36 months
Safety Issue:
Description:Objective response rate is calculated as the number of participants with best objective response [complete response (CR) or partial response (PR) determined by Investigator assessment based on Response Evaluation Criteria In Solid Tumors (RECIST) version 1.1], divided by the number of participants in the analysis population.
Measure:Change from baseline in size of target lesion(s)
Time Frame:within 36 months
Safety Issue:
Description:
Measure:Duration of response (DOR)
Time Frame:within 36 months
Safety Issue:
Description:DOR is defined as the time from documentation of tumor response [either CR or PR] to disease progression
Measure:Disease control rate (DCR)
Time Frame:first dose to 36 months
Safety Issue:
Description:DCR is defined as the sum of CR rate, PR rate, and stable disease (SD) rate
Measure:Progression-free survival (PFS)
Time Frame:baseline to objective disease progression or death from any cause (within 36 months)
Safety Issue:
Description:PFS is defined as the time from the date of the first dose to the earlier of the dates of the first objective documentation of radiographic PD, or death due to any cause
Measure:Overall survival (OS)
Time Frame:baseline to death from any cause (within 36 months)
Safety Issue:
Description:

Details

Phase:Phase 1
Primary Purpose:Interventional
Overall Status:Recruiting
Lead Sponsor:Daiichi Sankyo, Inc.

Trial Keywords

  • Oncology
  • Advanced Non-small Cell Lung Cancer
  • Inoperable Non-small Cell Lung Cancer
  • Metastatic
  • Non-resectable
  • Epidermal growth factor receptor
  • EGFR

Last Updated

March 1, 2018