Descrizione riassuntiva della sperimentazione (Fonte di dati: BASEC)
Ziel dieser Studie ist es, herauszufinden, ob das Medikament NIS793 mit oder ohne Spartalizumab in Kombination mit einer Standard-Chemotherapie (Gemcitabin und nab-Paclitaxel) bei Patienten mit metastasiertem Bauchspeicheldrüsenkrebs sicher und wirksam ist.
NIS793 und Spartalizumab sind vom Schweizerischen Heilmittelinstitut Swissmedic und anderen Gesundheitsbehörden für die Behandlung von Menschen mit Bauchspeicheldrüsenkrebs noch nicht zugelassen.
Gemcitabin und nab-Paclitaxel sind Chemotherapeutika. Sie sind von Swissmedic und anderen Gesundheitsbehörden für die Behandlung von verschiedenen Arten von Krebs, darunter auch Bauchspeicheldrüsenkrebs, zugelassen.
Diese Studie besteht aus zwei Teilen:
Teil 1: In diesem Teil der Studie wird eine kleine Anzahl von Patienten (ca. 6) NIS793 mit Spartalizumab in Kombination mit einer Standard-Chemotherapie (Gemcitabin und nab-Paclitaxel) erhalten. Der Zweck dieses Teils besteht darin, herauszufinden, ob die Studienbehandlung sicher ist.
Teil 2: Wenn sich die Studienbehandlung in Teil 1 der Studie als sicher erwiesen hat, beginnt Teil 2 der Studie. In diesem Teil der Studie werden die Patienten chancengleich einem der drei Behandlungsarme zugeteilt:
• Arm 1: NIS793 + Spartalizumab + Gemcitabin + nab-Paclitaxel
• Arm 2: NIS793 + Gemcitabin + nab-Paclitaxel
• Arm 3: Gemcitabin + nab-Paclitaxel
Rund 156 Patienten werden in verschiedenen Studienzentren rund um die Welt an der Studie teilnehmen, davon ungefähr 10 in der Schweiz.
Malattie studiate(Fonte di dati: BASEC)
Metastasierter Bauchspeicheldrüsenkrebs
Health conditions
(Fonte di dati: WHO)
Pancreatic ductal adenocarcinoma
MedDRA version: 21.0Level: LLTClassification code 10033604Term: Pancreatic cancerSystem Organ Class: 100000004864;Therapeutic area: Diseases [C] - Cancer [C04]
Malattia rara
(Fonte di dati: BASEC)
No
Interventi esaminati (p. es. medicamento, terapia, campagna)
(Fonte di dati: BASEC)
Alle Studienmedikamente werden als Infusionen in eine Vene verabreicht:
• Gemcitabin und nab-Paclitaxel an den Tagen 1, 8 und 15 jedes 28-tägigen Zyklus
• NIS793 an den Tagen 1 und 15 jedes 28-tägigen Zyklus
• Spartalizumab am Tag 1 jedes 28-tägigen Zyklus
Interventions
(Fonte di dati: WHO)
Product Code: NIS793
Pharmaceutical Form: Powder for solution for infusion
INN or Proposed INN: Not yet defined
Current Sponsor code: NIS793
Other descriptive name: NIS793
Concentration unit: mg milligram(s)
Concentration type: equal
Concentration number: 100-
Product Name: Spartalizumab
Product Code: PDR001
Pharmaceutical Form: Concentrate for solution for infusion
INN or Proposed INN: Spartalizumab
Current Sponsor code: PDR001
Other descriptive name: PDR001
Concentration unit: mg/ml milligram(s)/millilitre
Concentration type: equal
Concentration number: 25-
Product Name: nab-paclitaxel
Pharmaceutical Form: Powder for solution for infusion
INN or Proposed INN: Paclitaxel
CAS Number: 33069-62-4
Other descriptive name: PACLITAXEL ALBUMIN-BOUND
Concentration unit: mg/ml milligram(s)/millilitre
Concentration type: equal
Concentration number: 5-
Product Name: gemcitabine
Pharmaceutical Form: Concentrate for solution for infusion
INN or Proposed INN: GEMCITABINE
CAS Number: 95058-81-4
Other descriptive name: gemcitabine
Concentration unit: mg/ml milligram(s)/millilitre
Concentration type: equal
Concentration number: 40-
Criteri per la partecipazione alla sperimentazione
(Fonte di dati: BASEC)
- Männliche oder weibliche Patienten ab 18 Jahre
- Patienten mit metastasiertem Bauchspeicheldrüsenkrebs, die noch keine Therapie für Ihre Erkrankung erhalten haben
Criteri di esclusione
(Fonte di dati: BASEC)
- Patienten, die (unkontrolierte) Hirnmetastasen haben
Inclusion/Exclusion Criteria
(Fonte di dati: WHO)
Gender:
Female: yes
Male: yes
Inclusion criteria:
Participants with histologically or cytologically confirmed treatment na?ve metastatic adenocarcinoma of the pancreas with measurable disease per RECIST 1.1.
Participants must have a site of disease amenable to biopsy, be candidate for tumor biopsy, and must be willing to undergo a tumor biopsy at screening and during therapy on the study.
ECOG performance status = 1
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range 62
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range 94
Exclusion criteria:
Previous radiotherapy, surgery (note: placement of biliary stent is allowed), chemotherapy or investigational therapy for the treatment of metastatic disease. Participants having received previous chemotherapy in the adjuvant setting
Participants with MSI-H pancreatic adenocarcinoma
Participants with a diagnosis of pancreatic neuroendocrine tumors (NETs), acinar, or islet cell tumors
Participants amenable to potentially curative resection
Presence of symptomatic CNS metastases or CNS metastases that require local CNS-directed therapy
History of severe hypersensitivity reactions to other monoclonal antibodies
Malignant disease other than that being treated in the study
Systemic chronic steroid therapy (>10mg/day prednisone or equivalent) or any immunosuppressive therapy
Known history of testing positive for HIV infection
Active HBV and HCV infection
Use of any live vaccines against infectious diseases within 4 weeks of initiation of study treatment
Active, known or suspected autoimmune disease
History of or current pneumonitis or interstitial lung disease
-
Altre informazioni sulla sperimentazione
Data di registrazione della sperimentazione
16 lug 2020
Inserimento del primo partecipante
9 nov 2020
Stato di reclutamento
Not Recruiting
Titolo scientifico
(Fonte di dati: WHO)
A phase II, open label, randomized, parallel arm study of NIS793 (with and without spartalizumab) in combination with SOC chemotherapy gemcitabine/nab-paclitaxel, and gemcitabine/nab-paclitaxel alone in first-line metastatic pancreatic ductal adenocarcinoma (mPDAC)
Tipo di sperimentazione
(Fonte di dati: WHO)
Interventional clinical trial of medicinal product
Disegno della sperimentazione
(Fonte di dati: WHO)
Controlled: no Randomised: yes Open: yes Single blind: no Double blind: no Parallel group: no Cross over: no Other: no If controlled, specify comparator, Other Medicinial Product: Placebo: Other: Number of treatment arms in the trial: 4
Fase
(Fonte di dati: WHO)
Human pharmacology (Phase I): noTherapeutic exploratory (Phase II): yesTherapeutic confirmatory - (Phase III): noTherapeutic use (Phase IV): no
Punti finali primari
(Fonte di dati: WHO)
Main Objective: Safety Run-in part:
? To assess the safety and tolerability of NIS793 with spartalizumab in combination with gemcitabine/nab-paclitaxel.
Randomized part:
? To evaluate the Progression Free Survival (PFS) per Investigator assessment of NIS793 with and without spartalizumab in combination with gemcitabine/nab-paclitaxel versus SOC chemotherapy gemcitabine/nab-paclitaxel.
? To evaluate the PFS of NIS793 with gemcitabine/nab-paclitaxel versus gemcitabine/nab-paclitaxel
;Secondary Objective: Randomized part:
? To evaluate the safety and tolerability of NIS793 with and without spartalizumab in combination with gemcitabine/nab-paclitaxel versus gemcitabine/nab-paclitaxel
? To assess the preliminary anti-tumor activity of NIS793 with and without spartalizumab in combination with gemcitabine/nab-paclitaxel versus gemcitabine/nab-paclitaxel
? To assess Overall Survival (OS) of NIS793 with and without spartalizumab in combination with gemcitabine/nab-paclitaxel versus gemcitabine/nab-paclitaxel
? To assess the CD8 and PD-L1 status of the participants at screening and on treatment versus gemcitabine/nab-paclitaxel
? To characterize the incidence of immunogenicity of NIS793 and spartalizumab in combination with gemcitabine/nab-paclitaxel
? To characterize the pharmacokinetics (PK) of NIS793, spartalizumab, gemcitabine/nab-paclitaxel in combination treatment or alone (gemcitabine/nab-paclitaxel)
;Primary end point(s): Safety Run-in part:
1) Incidence of DLTs during the first 4 weeks of treatment
2) Safety: Incidence and severity of treatment emergent AEs and SAEs, changes between baseline and post-baseline laboratory parameters, vital signs, and ECG parameters
3) Tolerability: Dose interruptions, reductions and dose intensity
Randomized part:
4) Progression-free survival based on Response Evaluation Criteria in Solid Tumors (RECIST1.1) as per local Investigator?s review;Timepoint(s) of evaluation of this end point: 1) DLT observation period 4 weeks
2), 3), 4) end of study
Punti finali secondari
(Fonte di dati: WHO)
Secondary end point(s): Incidence and severity of AEs and SAEs, including changes in laboratory values, vital signs and ECGs, dose interruptions, reductions, and dose intensity
Overall response rate (ORR), Duration of response (DOR), Time to Progression (TTP) RECIST 1.1 as per local Investigator?s review
Overall Survival (OS)
Change from baseline in CD8 and PD-L1 IHC related markers
Antidrug antibodies (ADA) prevalence at baseline and ADA incidence on-treatment (anti-NIS793 and anti-spartalizumab)
Pharmacokinetic parameters (e.g. Ctrough, Cmax, AUClast)
PK concentration time profiles
;Timepoint(s) of evaluation of this end point: as per protocol Table 8-1
Contatto per informazioni
(Fonte di dati: WHO)
Novartis Pharma AG
Risultati della sperimentazione
(Fonte di dati: WHO)
Sintesi dei risultati
A phase II, open label, randomized, parallel arm study of NIS793 (with and without spartalizumab) in combination with SOC chemotherapy gemcitabine/nab-paclitaxel, and gemcitabine/nab-paclitaxel alone in first-line metastatic pancreatic ductal adenocarcinoma (mPDAC)
Collegamento ai risultati nel registro primario
ancora nessuna informazione disponibile
Informazioni sulla disponibilità dei dati dei singoli partecipanti
ancora nessuna informazione disponibile
Siti di esecuzione della sperimentazione
Siti di esecuzione in Svizzera
(Fonte di dati: BASEC)
San Gallo, Zurigo
Paesi di esecuzione
(Fonte di dati: WHO)
Australia, Austria, Belgium, Canada, Czech Republic, Finland, France, Germany, Italy, Japan, Singapore, Spain, Switzerland, Taiwan, United Kingdom, United States
Contatto per maggiori informazioni sulla sperimentazione
Dati della persona di contatto in Svizzera
(Fonte di dati: BASEC)
Patrick Grabher
+41 79 330 70 18
patrick.grabher@novartis.com
Contatto per informazioni generali
(Fonte di dati: WHO)
Information&Communication M?dicales
8/10 rue Henry Sainte Claire Deville, CS 40150
Novartis Pharma S.A.S
+33 1 5547 6600
icm.phfr@novartis.com
Contatto per informazioni scientifiche
(Fonte di dati: WHO)
Information&Communication M?dicales
8/10 rue Henry Sainte Claire Deville, CS 40150
Novartis Pharma S.A.S
+33 1 5547 6600
icm.phfr@novartis.com
Autorizzazione da parte della commissione d’etica (Fonte di dati: BASEC)
Nome della commissione d’etica che rilascia l’autorizzazione (nel caso di studi multicentrici solo la commissione direttiva)
Ethikkommission Ostschweiz (EKOS)
Data di autorizzazione da parte della commissione d’etica
18.09.2020
Altri numeri di identificazione delle sperimentazioni
Numero di identificazione della sperimentazione della commissione d’etica (BASEC-ID)
(Fonte di dati: BASEC)
2020-01797
Secondary ID (Fonte di dati: WHO)
CNIS793B12201
2020-000349-14-FI
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