In Phase IIa, dose-escalation study to determine the optimum tolerated dose and a recommended Phase IIb (RPIIb) dose in combination with pembrolizumab in subjects with recurrent or metastatic squamous cell carcinoma of the head and neck who have failed platinum or a platinum containing regimen. In Phase IIb, randomized control study between NC-6004 in combination with pembrolizumab versus pembrolizumab alone in the same subject population as Part 1 at the RPIIb dose identified in PIIa.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
136
NC-6004 should be administered to subjects once every 3 weeks. On Day 1 of each treatment cycle NC-6004 will be administered first followed by pembrolizumab.
The recommended dose of pembrolizumab is 200 mg administered as an IV infusion over 30 minutes every 3 weeks.
0603
Osijek, Croatia
RECRUITING0601
Zagreb, Croatia
Determine the Recommended Phase (RPII) dose (mg/m2) of NC-6004 in combination with pembrolizumab
In PIIa portion, to determine RPII dose of NC-6004 in combination with pembrolizumab
Time frame: 1 year
Compare median Progression Free Survival (PFS) between NC-6004 +pembrolizumab and pembrolizumab alone
In PIIb portion, to compare PFS between NC-6004 plus pembrolizumab and pembrolizumab alone.
Time frame: 1 year
Compare median Overall Survival (OS) between NC-6004 +pembrolizumab and pembrolizumab alone
In PIIb portion, to compare OS rate between NC-6004 plus pembrolizumab and pembrolizumab alone.
Time frame: 2 years
Compare overall response (complete response and partial response) rate between NC-6004 +pembrolizumab and pembrolizumab alone
In PIIb portion, to ORR between NC-6004 plus pembrolizumab and pembrolizumab alone
Time frame: 1 year
Compare duration of response between NC-6004 +pembrolizumab and pembrolizumab alone
In PIIb portion, to compare DOR between NC-6004 plus pembrolizumab and pembrolizumab alone
Time frame: 1 year
Compare time to response between NC-6004 +pembrolizumab and pembrolizumab alone
In PIIb portion, to compare TTR between NC-6004 plus pembrolizumab and pembrolizumab alone
Time frame: 1 year
Safety and tolerability as measured by severity of Adverse Events (AEs)
The safety endpoints for this study are the incidence and severity of AEs in accordance with the NCI CTCAE and the occurrence of SAEs and treatment discontinuations due to AEs
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
0602
Zagreb, Croatia
RECRUITING0701
Brno, Czechia
RECRUITING0702
Hradec Králové, Czechia
RECRUITING0703
Olomouc, Czechia
RECRUITING0104
Budapest, Hungary
RECRUITING0105
Debrecen, Hungary
RECRUITING0103
Kecskemét, Hungary
RECRUITING0101
Pécs, Hungary
RECRUITING...and 14 more locations
Time frame: 1 year
Assess the Maximum Plasma Concentration (Cmax) of NC-6004 in combination with pembrolizumab
Assess PK parameters of the Maximum Plasma Concentration (Cmax)
Time frame: 1 year
Assess the Time to Maximum Concentration (Tmax) of NC-6004 in combination with pembrolizumab
Assess PK parameters of Time to Maximum Concentration (Tmax)
Time frame: 1 year
Assess the Area Under the Concentration (AUC) of NC-6004 in combination with pembrolizumab
Assess PK parameters of Area Under the Concentration (AUC)
Time frame: 1 year
Assess the Half-life(T½) of NC-6004 in combination with pembrolizumab
Assess PK parameters of Half-life(T½)
Time frame: 1 year
Assess the Clearance (CL) of NC-6004 in combination with pembrolizumab
Assess PK parameters of Clearance (CL)
Time frame: 1 year
Assess the Volume of Distribution (V) of NC-6004 in combination with pembrolizumab
Assess PK parameters of Volume of Distribution (V)
Time frame: 1 year