Immunotherapy With Nivolumab or Nivolumab Plus Ipilimumab vs. Double Placebo for Stage IV Melanoma w. NED

Malignant Melanoma Clinical Trial

Official title:

A Phase II Randomized, Double-Blind Trial of Immunotherapy With Nivolumab or Nivolumab Plus Ipilimumab Versus Double-Placebo Control as a Post-Surgical/Post-Radiation Treatment for Stage IV Melanoma With No Evidence of Disease

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02523313
• Other study ID #: IMMUNED
• Status: Completed
• Phase: Phase 2
• Start date: September 2, 2015
• Est. completion date: June 27, 2021

Study information

• Verified date: December 2021
• Source: University Hospital, Essen
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a prospective, double-blind placebo-controlled, multicenter, randomized phase II trial testing the adjuvant immunotherapy with Nivolumab plus Ipilimumab Placebo or Nivolumab plus Ipilimumab versus Double Placebo Control as a post-surgical/post-radiation treatment for stage IV melanoma with no evidence of disease (NED).

Description:

This study will allow for direct comparison of the clinical benefit provided by Nivolumab monotherapy or Nivolumab combined with Ipilimumab versus double placebo control. Furthermore, it will also allow for direct comparison of the respective safety profiles of Nivolumab monotherapy or Nivolumab combined with Ipilimumab. Nivolumab monotherapy was chosen as one of the experimental arms because of a favourable risk-benefit ratio assessed in the large Phase 1 study (MDX1106-03/CA209-003). The combination of Nivolumab and Ipilimumab was chosen as an experimental arm because of the preliminary evidence from the Phase 1 study CA209-004 suggesting synergy between Nivolumab and Ipilimumab resulting in a higher frequency of patients with increased tumour burden reduction. Evaluating both Nivolumab monotherapy and the combination of Nivolumab and Ipilimumab will provide clinical data allowing clinicians to select the appropriate treatment for each patient based on their individual risk-benefit ratio.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 167
• Est. completion date: June 27, 2021
• Est. primary completion date: June 27, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Stage IV melanoma arising from a primary cutaneous site or metastatic from an unknown primary site with no evidence of disease (NED) after surgery or radiation therapy (conducted within 8 weeks before enrolment)

• Signed written informed consent

• Known BRAF status

• Subjects must be willing and able to comply with scheduled visits, treatment schedule, laboratory testing, and other requirements of the study

• Minimum life expectancy of five years excluding their melanoma diagnosis

• ECOG performance status of 0 or 1

• Tumor tissue from the resected site of disease must be provided for biomarker analyses. In order to be randomized a subject must have a PD-L 1 expression classification (positive (= 5% tumor cells expressing PD-L1) or negative (< 5% tumor cells expressing PD-L1)). If an insufficient amount of tumor tissue from the resected site is provided for analysis, acquisition of additional archived tumor tissue (block and/or slides) for the biomarker analyses is required.

• Prior radiotherapy must have been completed at least 2 weeks prior to study drug administration

• Required laboratory values

• Negative pregnancy test for female subjects and effective contraception (Pearl-Index <1) for both male and female subjects if the risk of conception exists

Exclusion Criteria:

• History of primary uveal or mucosal melanoma

• Prior therapy with CTLA4 or PD1 antibodies

• The patient has psychiatric or addictive disorders that may compromise his/her ability to give informed consent or to comply with the trial procedures.

• Lack of availability for clinical follow-up assessments.

• Any immunosuppressive therapy given within the past 30 days prior to study drug administration (excluding physiologic steroid hormone replacement)

• Other malignancies within the past five years requiring treatment except basal or squamous skin carcinomas or carcinoma in situ of the cervix

• Serious cardiac, gastrointestinal, hepatic or pulmonary disease reducing life expectancy to less than five years

• Patients with serious intercurrent illness, requiring hospitalization.

• Other serious illnesses, e.g., serious infections requiring antibiotics or bleeding disorders.

• The patient is known to be positive for Human Immunodeficiency Virus (HIV) or other chronic infections (HBV, HCV) or has another confirmed or suspected immunosuppressive or immunodeficient condition.

• Known hypersensitivity reaction to any of the components of study treatment

• Pregnancy (absence to be confirmed by ß-HCG urinary test, minimum sensitivity 25IU/L or equivalent units of HCG)) or lactation period

• Women of childbearing potential (WOCBP): Refusal or inability to use effective means of contraception (Pearl-Index <1). WOCBP will be instructed to adhere to contraception until 31 weeks after the last dose of investigational product

• Men who are sexually active with WOCBP must use any contraceptive method with a failure rate of less than 1% per year (Pearl-Index <1). Men receiving Nivolumab and who are sexually active with WOCBP will be instructed to adhere to contraception until 31 weeks after the last dose of investigational product

• Known alcohol or drug abuse

• Participation in another clinical study and use of any investigational or non-registered product (drug or vaccine) within the 30 days before registration

• Significant disease or condition which, in the investigator's opinion, would exclude the patient from the study

• Legal incapacity or limited legal capacity

Related Conditions & MeSH terms

• Malignant Melanoma
• Melanoma

Intervention

Drug:
• Nivolumab + Placebo
Nivolumab will be applied at a dose of 3 mg/kg given as IV infusion every 2 weeks for up to 1 year after initial dosing or until PD + Placebo instead of Ipilimumab on weeks 1, 4, 7 and 10 + Placebo instead of Nivolumab on weeks 4 and 10.
• Nivolumab + Ipilimumab
Nivolumab (1 mg/kg) and Ipilimumab (3 mg/kg) will be applied as IV infusion every 3 weeks for 4 doses. Both study drugs are to be administered on the same day over the first 12 weeks + Nivolumab-Placebo on weeks 3, 5, 9 and 11. After week 12 Nivolumab is given as maintenance and will be applied at a dose of 3 mg/kg IV every 2 weeks for up to 1 year after initial dosing (of the combination) or until PD.
• Double Placebo Control
Placebo instead of Nivolumab and Placebo instead of Ipilimumab will be applied as IV infusion every 3 weeks for 4 doses. Both placebos are to be administered on the same day over the first 12 weeks + Placebo instead of Nivolumab on weeks 3, 5, 9 and 11. After week 12 Placebo instead of Nivolumab is given as maintenance and will be applied intravenously every 2 weeks for up to 1 year after initial dosing (of the combination) or until PD.

Locations

Country	Name	City	State
Germany	Charité Berlin	Berlin
Germany	Elbe Klinikum Buxtehude	Buxtehude
Germany	Universitätsklinikum Dresden	Dresden
Germany	HELIOS Klinikum Erfurt	Erfurt
Germany	Studienzentrum Hautklinik Universitätsklinikum Essen (AöR) Klinik für Dermatologie	Essen
Germany	SRH Wald-Klinikum Gera GmbH	Gera
Germany	Medizinische Hochschule Hannover	Hannover
Germany	Universitätrsklinikum Heidelberg Dermatologie / NCT	Heidelberg
Germany	SLK Kliniken Heilbronn GmbH	Heilbronn
Germany	Universitäts-Hautklinik Kiel Klinik f. Dermatologie, Venerologie u. Allergologie	Kiel
Germany	Universitätsklinikum Leipzig Klinik u. Poliklinik f. Dermatologie, Venerologie u. Allergologie	Leipzig
Germany	UKSH Campus Lübeck	Lübeck
Germany	Klinikum der Stadt Ludwigshafen	Ludwigshafen
Germany	Universitätsklinikum Mainz Hautklinik und Polklinik	Mainz
Germany	Klinik für Dermatologie, Venerologie und Allergologie UMM - Universitätsmedizin Mannheim	Mannheim
Germany	Johannes Wesling Klinikum Minden Hautklinik	Minden
Germany	Universitätsklinikum München (LMU)	München
Germany	Fachklinik Hornheide	Münster
Germany	Universitätsklinikum Regensburg	Regensburg
Germany	Universitätshautklinik Tübingen	Tübingen

Sponsors (1)

Lead Sponsor	Collaborator
Prof. Dr. med. Dirk Schadendorf

Country where clinical trial is conducted

Germany, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Safety / Toxicity All adverse events = Grade 3 according to CTCAE Version 4.0 criteria	All adverse events = Grade 3 according to CTCAE Version 4.0 criteria, that are related to the administration of the investigational agents will be assessed	until 90 days after discontinuation of dosing
Primary	Efficacy of adjuvant immunotherapy with Nivolumab alone or in combination with Ipilimumab (Recurrence-free survival)	Recurrence-free survival (RFS) defined as the time from date of randomization until the date of the first recurrence (local or distant metastasis), new primary melanoma or death from any cause, whichever occurs first.	24 months after the last patient ended treatment
Secondary	Overall survival (OS)	The OS of a patient is defined as the time from date of randomization until date of death.	24 months after the last patient ended treatment
Secondary	Time to recurrence (TTR)	The TTR of a patient is defined as the time from date of randomization until date of disease recurrence (local or distant metastasis) or melanoma-related death.	24 months after the last patient ended treatment
Secondary	Progression/recurrence free survival 2 (PRFS2) for crossover patients of Arm C	The PRFS2 is defined as time from date of randomization until the date of first disease progression per RECIST 1.1 beyond the initial unresectable disease recurrence, the date of second recurrence in patients without evidence of disease after surgery of a resectable first recurrence or the date of death, whichever occurs first.	24 months after the last patient ended treatment