Phase 2
N=55
A Study of AMNN107 in the Treatment of Metastatic and/or Inoperable Melanoma Harboring a c-Kit Mutation
Melanoma
Bottom Line
View on ClinicalTrials.gov: NCT01028222 ↗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
| Outcome | Result | p-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.
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.