Mode
Text Size
Log in / Sign up
Phase 2 N=55 Prevention

A Study of AMNN107 in the Treatment of Metastatic and/or Inoperable Melanoma Harboring a c-Kit Mutation

Melanoma

Enrolled (actual)
55
Serious AEs
26.2%
Results posted
Nov 2015
Primary outcome: Primary: Overall Response Rate (ORR) — 11; 3 Participants

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
Nilotinib (Drug); DTIC (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Novartis Pharmaceuticals
Primary completion
Dec 2014

Outcome Measures

OutcomeResultp-value
PRIMARY
Overall Response Rate (ORR)
11; 3
SECONDARY
Durable Overall Response Rate (DORR)
11; 3
SECONDARY
Progression Free Survival (PFS)
4.2; 4.2
SECONDARY
Overall Survival (OS)
18.0; 22.8
SECONDARY
Time to Objective Response (TOR)
NA; NA
SECONDARY
Disease Control Rate (DCR)
20; 7
SECONDARY
PFS Rate
34.6; 23.1
SECONDARY
OS Rate
63.6; 66.7

Summary

The purpose of this study is to determine whether nilotinib is efficacious in the treatment of metastatic and/or inoperable melanoma harboring a c-Kit mutation.

Eligibility Criteria

Inclusion Criteria

  • Histologically confirmed mucosal or acral 2. Presence of a c-Kit mutation of exon 9, 11 or 13, or mutations Y822D and mutations D820Y, Y823D of exon 17, as confirmed by the central laboratory 3. Stage III unresectable or stage IV disease 4. The presence of one or more measurable lesions as detected by radiological or photographic methods and assessed according to RECIST 1.0. Lesions must have a size of at least 10mm at longest diameter (using a slice thickness of 5 mm)or double the slice thickness to be considered a target lesion. Target lesions should not be selected in previously irradiated fields unless there is clear evidence of progression 5. WHO performance status 0 - 2

Exclusion Criteria

  • C-Kit mutation of exons 17(except mutations D820Y, Y822D or Y823D) or any other exon not allowed by the inclusion criteria
  • Patients with c-Kit amplifications only and no mutation
  • Patients with any history of brain metastases
  • Patients who have had any prior treatment with TKIs
  • Patients receiving medications or herbal extracts which interfere with nilotinib metabolism which are not discontinued by the time of the baseline visit
  • Acute or chronic liver or renal disease considered unrelated to melanoma

Other protocol-defined inclusion/exclusion criteria may have applied.

View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01028222). 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