A Phase I/II Study of DYP688 in Patients With Metastatic Uveal Melanoma and Other GNAQ/11 Mutant Melanomas

• ClinicalTrials.gov Identifier: NCT05415072
• Recruitment Status: Recruiting
• First Posted: June 10, 2022
• Last Update Posted: March 22, 2023
• Sponsor: Novartis Pharmaceuticals
• Information provided by (Responsible Party): Novartis ( Novartis Pharmaceuticals )

Tracking Information

• First Submitted Date: June 8, 2022
• First Posted Date: June 10, 2022
• Last Update Posted Date: March 22, 2023
• Actual Study Start Date: July 4, 2022
• Estimated Primary Completion Date: March 12, 2026 (Final data collection date for primary outcome measure)

Current Primary Outcome Measures (submitted: June 8, 2022)

• Phase I (Dose Escalation): Incidence and severity of dose limiting toxicities (DLTs) during the first 28 days of treatment. [ Time Frame: 28 days ]
  A DLT is defined as an adverse event or abnormal laboratory value of Common Terminology Criteria for Adverse Events (CTCAE) grade ≥ 3 assessed as unrelated to disease, disease progression, intercurrent illness, or concomitant medications that occurs within the first cycle of treatment with DYP688. Other clinically significant toxicities may be considered to be DLTs, even if not CTCAE grade 3 or higher.
• Phase I (Dose Escalation): Incidence and severity of adverse events (AEs) and serious adverse events (SAEs) [ Time Frame: 9 months ]
  Assessment of safety of DYP688 as a single agent
• Phase I (Dose Escalation): Frequency of dose interruptions, reductions, and discontinuations [ Time Frame: 9 months ]
  Assessment of tolerability of DYP688 as a single agent
• Phase II: Overall Response rate (ORR) per RECIST 1.1 [ Time Frame: 17 months ]
  ORR in Phase II will be evaluated by central review per RECIST 1.1.

• Original Primary Outcome Measures: Same as current

Current Secondary Outcome Measures (submitted: January 31, 2023)

• Phase I and Phase II: PK profile of DYP688 - Area under the concentration-time curve (AUC) [ Time Frame: 26 months ]
  Pharmacokinetic (PK) parameters will be determined by non-compartmental methods using pharmacokinetic profile of DYP688.
• Phase I and Phase II: PK profile of DYP688 - Peak concentration (Cmax) [ Time Frame: 26 months ]
  Pharmacokinetic parameters will be determined by non-compartmental methods using pharmacokinetic profile of DYP688.
• Phase I and Phase II: PK profile of DYP688 - Total body clearance (CL) [ Time Frame: 26 months ]
  Pharmacokinetic parameters will be determined by non-compartmental methods using pharmacokinetic profile of DYP688.
• Phase I and Phase II: PK profile of DYP688 - Elimination half-life [ Time Frame: 26 months ]
  Pharmacokinetic parameters will be determined by non-compartmental methods using pharmacokinetic profile of DYP688.
• Phase I and Phase II: Prevalence and incidence of anti-DYP688 antibodies [ Time Frame: 26 months ]
  Assess of immunogenicity (IG) of DYP688 as a single agent
• Phase I (Dose Escalation): Best Overall Response (BOR) per RECIST v1.1 [ Time Frame: 9 months ]
  Evaluation of preliminary anti-tumor activity of DYP688 as a single agent
• Phase I (Dose Escalation): Overall Response Rate (ORR) per RECIST v1.1 [ Time Frame: 17 months ]
  Evaluation of preliminary anti-tumor activity of DYP688 as a single agent
• Phase II: Duration of response (DoR) per RECIST v1.1 [ Time Frame: 17 months ]
  Evaluation of anti-tumor activity of DYP688 as a single agent
• Phase II: Progression free survival (PFS) per RECIST v1.1 [ Time Frame: 17 months ]
  Evaluation of anti-tumor activity of DYP688 as a single agent
• Phase II: Disease Control Rate (DCR) per RECIST v1.1 [ Time Frame: 17 months ]
  Evaluation of anti-tumor activity of DYP688 as a single agent
• Phase II: Overall Survival (OS) [ Time Frame: 17 months ]
  Evaluation of the effect of DYP688 as a single agent on overall survival
• Phase II: Incidence and severity of adverse events (AEs) and serious adverse events (SAEs) [ Time Frame: 17 months ]
  Assessment of safety of DYP688 as a single agent
• Phase II: Frequency of dose interruptions, reductions, and discontinuations [ Time Frame: 17 months ]
  Assessment of tolerability of DYP688 as a single agent

Original Secondary Outcome Measures (submitted: June 8, 2022)

• Phase I and Phase II: PK profile of DYP688 - Area under the concentration-time curve (AUC) [ Time Frame: 26 months ]
  Pharmacokinetic (PK) parameters will be determined by non-compartmental methods using pharmacokinetic profile of DYP688.
• Phase I and Phase II: PK profile of DYP688 - Peak concentration (Cmax) [ Time Frame: 26 months ]
  Pharmacokinetic parameters will be determined by non-compartmental methods using pharmacokinetic profile of DYP688.
• Phase I and Phase II: PK profile of DYP688 - Total body clearance (CL) [ Time Frame: 26 months ]
  Pharmacokinetic parameters will be determined by non-compartmental methods using pharmacokinetic profile of DYP688.
• Phase I and Phase II: PK profile of DYP688 - Elimination half-life [ Time Frame: 26 months ]
  Pharmacokinetic parameters will be determined by non-compartmental methods using pharmacokinetic profile of DYP688.
• Phase I (Dose Escalation): Prevalence and incidence of anti-DYP688 antibodies [ Time Frame: 9 months ]
  Assess of immunogenicity (IG) of DYP688 as a single agent
• Phase I (Dose Escalation): Best Overall Response (BOR) per RECIST v1.1 [ Time Frame: 9 months ]
  Evaluation of preliminary anti-tumor activity of DYP688 as a single agent
• Phase I (Dose Escalation): Overall Response Rate (ORR) per RECIST v1.1 [ Time Frame: 17 months ]
  Evaluation of preliminary anti-tumor activity of DYP688 as a single agent
• Phase II: Duration of response (DoR) per RECIST v1.1 [ Time Frame: 17 months ]
  Evaluation of anti-tumor activity of DYP688 as a single agent
• Phase II: Progression free survival (PFS) per RECIST v1.1 [ Time Frame: 17 months ]
  Evaluation of anti-tumor activity of DYP688 as a single agent
• Phase II: Disease Control Rate (DCR) per RECIST v1.1 [ Time Frame: 17 months ]
  Evaluation of anti-tumor activity of DYP688 as a single agent
• Phase II: Overall Survival (OS) [ Time Frame: 17 months ]
  Evaluation of overall survival with DYP688 as a single agent
• Phase II: Incidence and severity of adverse events (AEs) and serious adverse events (SAEs) [ Time Frame: 17 months ]
  Assessment of safety of DYP688 as a single agent
• Phase II: Frequency of dose interruptions, reductions, and discontinuations [ Time Frame: 17 months ]
  Assessment of tolerability of DYP688 as a single agent

• Current Other Pre-specified Outcome Measures: Not Provided
• Original Other Pre-specified Outcome Measures: Not Provided

Descriptive Information

• Brief Title: A Phase I/II Study of DYP688 in Patients With Metastatic Uveal Melanoma and Other GNAQ/11 Mutant Melanomas
• Official Title: A Phase I/II, Multi-center, Open Label Study of DYP688 in Patients With Metastatic Uveal Melanoma (MUM) and Other GNAQ/11 Mutant Melanomas
• Brief Summary: 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.
• Detailed Description: 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.
• Study Type: Interventional
• Study Phase: Phase 1; Phase 2
• Study Design: Allocation: Non-Randomized; Intervention Model: Sequential Assignment; Masking: None (Open Label); Primary Purpose: Treatment
• Condition: Metastatic Uveal Melanoma

Intervention

Drug: DYP688

Single agent DYP688

Study Arms

• Experimental: Phase I: Dose Escalation
  Patients with metastatic uveal melanoma or other GNAQ/11 mutant melanomas
  Intervention: Drug: DYP688
• Experimental: Phase II: Tebe naive group
  Patients with metastatic uveal melanoma that has not received prior treatment with tebentafusp
  Intervention: Drug: DYP688
• Experimental: Phase II: Tebe pre-treated
  Patients with metastatic uveal melanoma that have been previously treated with tebentafusp
  Intervention: Drug: DYP688
• Experimental: Phase II: Non-uveal melanoma
  Optional Arm: To explore patients with non-uveal melanoma that harbor GNAQ or 11 mutations, based on emerging data from dose escalation
  Intervention: Drug: DYP688

• Publications *: Not Provided

Recruitment Information

• Recruitment Status: Recruiting
• Estimated Enrollment (submitted: June 8, 2022): 124
• Original Estimated Enrollment: Same as current
• Estimated Study Completion Date: March 13, 2026
• Estimated Primary Completion Date: March 12, 2026 (Final data collection date for primary outcome measure)

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.

Sex/Gender

• Sexes Eligible for Study: All

• Ages: 12 Years and older (Child, Adult, Older Adult)
• Accepts Healthy Volunteers: No

Contacts

Contact: Novartis Pharmaceuticals; 1-888-669-6682; novartis.email@novartis.com

Contact: Novartis Pharmaceuticals; +41613241111; novartis.email@novartis.com

• Listed Location Countries: Australia, France, Germany, Netherlands, Spain, Switzerland, United States

Administrative Information

• NCT Number: NCT05415072
• Other Study ID Numbers: CDYP688A12101; 2021-003380-95 ( EudraCT Number )
• Has Data Monitoring Committee: Yes

U.S. FDA-regulated Product

• Studies a U.S. FDA-regulated Drug Product: Yes
• Studies a U.S. FDA-regulated Device Product: No

IPD Sharing Statement

• Plan to Share IPD: Undecided

• Current Responsible Party: Novartis ( Novartis Pharmaceuticals )
• Original Responsible Party: Same as current
• Current Study Sponsor: Novartis Pharmaceuticals
• Original Study Sponsor: Same as current
• Collaborators: Not Provided
• Investigators: Not Provided
• PRS Account: Novartis
• Verification Date: March 2023