Mode
Text Size
Log in / Sign up
Phase 2 N=248 Randomized Treatment

Phase II Anetumab Ravtansine as 2nd Line Treatment for Malignant Pleural Mesothelioma (MPM)

Mesothelioma

Enrolled (actual)
248
Serious AEs
34.5%
Results posted
Jul 2020
Primary outcome: Primary: Progression-free Survival (PFS), [95% CI] — 4.3; 4.5 months — p=0.859125

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
Anetumab ravtansine (BAY94-9343) (Drug); Vinorelbine (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Bayer
Primary completion
May 2017

Outcome Measures

OutcomeResultp-value
PRIMARY
Progression-free Survival (PFS), [95% CI]
4.3; 4.5 0.859125
SECONDARY
Overall Survival (OS), [95% CI]
9.5; 11.6 0.655624
SECONDARY
Objective Response Rate (ORR)
8.4; 6.1
SECONDARY
Disease Control Rate (DCR)
73.5; 68.3
SECONDARY
Duration of Response (DOR)
7.4; 6.7
SECONDARY
Durable Response Rate (DRR)
7.2; 4.9
SECONDARY
Percentage of Participants With Confirmed Improvement of Symptoms Characteristic of Mesothelioma
22.5; 17.9 0.244
SECONDARY
Time to Worsening of Symptoms Characteristic of Mesothelioma
NA; NA 0.313747
SECONDARY
Time to Worsening of Pain
210; NA 0.378916
SECONDARY
Percentage of Participants With Confirmed Improvement of Pain
40.4; 32.7 0.214
SECONDARY
Percentage of Participant With Treatment-emergent Adverse Events (TEAEs)
99.4; 98.6; 88.3; 90.3; 34.4; 34.7
SECONDARY
Number of Deaths
10; 1
SECONDARY
Overall Survival (OS) - Addendum
9.5; 11.6

Summary

The main purpose of the 15743 study is to assess efficacy and safety of anetumab ravtansine versus vinorelbine in progression free survival in patients with stage IV mesothelin overexpressing malignant pleural mesothelioma (MPM). 210 eligible patients will be randomized to receive either anetumab ravtansine every three weeks or weekly vinorelbine. Treatment will continue until centrally confirmed disease progression or until another criterion is met for withdrawal from the study. Patients will enter follow up phase to capture safety and endpoint data as required. Efficacy will be measured by evaluating progression free survival from randomization. Radiological tumor assessments will be performed at defined time points until the patient's disease progresses. Blood samples will be collected for safety, pharmacokinetic and biomarker analysis. Archival or fresh biopsy tissue may also be collected for central pathology review and biomarkers.

Eligibility Criteria

Inclusion Criteria

  • Histological documentation of malignant pleural mesothelioma (MPM) overexpressing mesothelin
  • Unresectable locally advanced or metastatic MPM after locally confirmed progression on 1st line treatment with platinum in combination with pemetrexed.
  • Patients must have measurable disease
  • Eastern Cooperative Oncology Group Performance Status (ECOG PS) of 0 or 1
  • Life expectancy of at least 3 months.
  • Adequate bone marrow, liver and renal function
  • Left ventricular ejection fraction (LVEF) ≥ 50% or the lower limit of normal (LLN) according to local institution ranges of normality.

Exclusion Criteria

  • More than 1 previous systemic anti-cancer therapy line
  • Patients with corneal epitheliopathy or any eye disorder that may predispose the patients to this condition at the discretion of the investigator in consultation with the ophthalmologist.
  • Brain metastases, meningeal tumours or other metastases in the central nervous system
  • Evidence of history of bleeding diathesis.
  • Ongoing or active infection (bacterial, fungal, or viral) of National Cancer Institute's Common Terminology Criteria for Adverse Events (NCI-CTCAE) version 4.03 Grade > 2.
  • Pre-existing cardiac conditions
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02610140). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

Back to search