Study Description
This is a FIH, phase I/II, open label, multi-center study of DYP688 as a single agent.
The purpose of this study is to characterize the safety, tolerability, and anti-tumor
activity of DYP688 as a single agent in patients with metastatic uveal melanoma (MUM) and
other melanomas harboring GNAQ/11 mutations. This is a First in Human (FIH), phase I/II, open label, multi-center study of DYP688 as a
single agent. There will be two parts to this study: a phase I, dose escalation part
followed by a phase II part. Dose escalation will be conducted in patients with MUM and
other melanomas harboring GNAQ/11 mutations. Once the MTD and/or RD(s) is determined in
the dose escalation part, the study may continue with a phase II part. The phase II part
will be conducted in two groups of patients with MUM, a prior tebentafusp-treated group
and a tebentafusp-naïve group. In addition to MUM, a third group of patients with
non-uveal GNAQ/11 mutant melanomas may also be explored. This cohort may be opened based
on emerging data from the dose escalation part of the study.
Interventions
DYP688
Eligibility Criteria
Inclusion Criteria:
- Patients in the dose escalation part must be ≥ 18 years of age at the time of
informed consent (ICF) signature. In the phase II part, patients ≥ 12 years of age
at the time of informed consent may be eligible for enrollment (not applicable in
countries where enrollment is restricted by the local health authority to patients ≥
18 years of age). Patients must have a minimum weight of 40 kg.
- ECOG performance status ≤ 1 for patients ≥ 18 years of age; Karnofsky performance
status ≥ 70 for patients ≥ 16 and < 18 years of age; Lansky performance status ≥ 70
for patients ≥ 12 and < 16 years of age
- Patients must be suitable and willing to undergo study required biopsies according
to the treating institution's own guidelines and requirements. If a biopsy is not
medically feasible, exceptions may be considered after documented discussion with
Novartis.
For all patients in Dose Escalation
- MUM: uveal melanoma with histologically or cytologically confirmed metastatic
disease. Patient must be either treatment naive or have received any number of prior
lines and progressed on most recent therapy
- Non-MUM: advanced cutaneous or mucosal melanoma with histologically or cytologically
confirmed metastatic disease that has progressed following all standard therapies or
that has no satisfactory alternative therapies and has evidence of GNAQ/11 mutation
based on local data
For patients in Phase II
- Tebentafusp naïve group: Diagnosis of uveal melanoma with histologically or
cytologically confirmed metastatic disease that has progressed following standard
therapies or that has no satisfactory alternative therapies
- Tebentafusp pre-treated group: Diagnosis of uveal melanoma with histologically or
cytologically confirmed metastatic disease. Patients must be previously treated with
tebentafusp and have progressed
- Non-MUM: patients with diagnosis of cutaneous or mucosal melanomas harboring GNAQ/11
mutations based on local data, with histologically or cytologically confirmed
metastatic disease that has progressed following all standard therapies or that has
no satisfactory alternative therapies
Exclusion Criteria:
- Malignant disease, other than that being treated in this study.
- Active brain metastases, i.e. symptomatic brain metastases or known leptomeningeal
disease.
- Evidence of active bleeding or bleeding diathesis or significant coagulopathy
(including familial) or a medical condition requiring long term systemic
anticoagulation that would interfere with biopsies.
- History of anaphylactic or other severe hypersensitivity / infusion reactions to
ADCs or monoclonal antibodies, which in the opinion of the investigator may pose an
increased risk of serious infusion reaction.
- Treatment with any of the following anti-cancer therapies prior to the first dose of
study treatment within the stated timeframes:
- 2 weeks for fluoropyrimidine therapy
- 4 weeks for radiation therapy or limited field radiation for palliation within
≤ 2 weeks prior to the first dose of study treatment.
- 4 weeks or ≤ 5 half-lives (whichever is shorter) for chemotherapy or biological
therapy (including monoclonal antibodies) or continuous or intermittent small
molecule therapeutics or any other investigational agent.
- 6 weeks for cytotoxic agents with major delayed toxicities, such as
nitrosoureas and mitomycin C.
- 4 weeks for immuno-oncologic therapy, such as CTLA-4, PD-1, or PD-L1
antagonists.
- Clinically significant and / or uncontrolled heart disease such as congestive heart
failure requiring treatment (NYHA grade ≥ 2) or clinically significant arrhythmia
despite medical treatment.
Other protocol-defined inclusion/exclusion criteria may apply.
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