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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03568929
Other study ID # GS-EU-313-4172
Secondary ID EUPAS19618
Status Completed
Phase
First received
Last updated
Start date May 25, 2018
Est. completion date October 29, 2021

Study information

Verified date November 2021
Source Gilead Sciences
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The primary objective of this study is to assess the overall safety profile of idelalisib monotherapy in patients with refractory follicular lymphoma (FL).


Recruitment information / eligibility

Status Completed
Enrollment 257
Est. completion date October 29, 2021
Est. primary completion date October 29, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Individuals who were or are being treated for refractory Follicular Lymphoma (FL) according to the product information for idelalisib and treatment guidelines in routine clinical practice. Exclusion Criteria: - Individuals included in clinical trials on idelalisib within the timeframe of this study.

Study Design


Intervention

Drug:
Idelalisib
Tablets administered according to the product information and treatment guidelines in routine clinical practice

Locations

Country Name City State
Belgium Ziekenhuis Netwerk Antwerpen Stuivenberg Hospital Antwerpen
France Centre Hospitalier Universitaire d'Amiens (CHU d'Amiens) - Hopital Nord Amiens Cedex 1
France Centre Hospitalier Bourg-en-Bresse Fleyriat Bourg-en-Bresse
France Centre Hospitalier de Cannes Cannes
France Hôpital Privé Sévigné Cesson-Sevigne
France Centre Hospitalier Chalon sur Saône William Morey Chalon-Sur-Saone
France Centre Hospitalier Universitaire Estaing Clermont-Ferrand
France CHU de Dijon Dijon
France Groupe Hospitalier Mutualiste de Grenoble - Institut Daniel Hollard Grenoble
France Centre Hospitalier Le Mans Le Mans
France Clinique Victor Hugo Le Mans Cedex 2
France Centre Hospitalier de Lens Lens
France Hôpital de la Conception Marseille
France Centre Hospitalier Régional d'Orléans Orléans
France Centre hospitalier de Perigueux Pessac
France Centre Hospitalier Lyon Sud Pierre Bénite Cedex
France Centre Hospitalier Universitaire de Poitiers Poitiers Cedex
France Hopital Bretonneau, Centre Henri Kaplan Tours
Germany Klinikum Frankfurt Hochst Frankfurt
Germany Universitätsmedizin Göttingen Göttingen
Germany Klinikum Südstadt Rostock Rostock
Germany Gemeinschaftspraxis für Hämatologie und Onkologie Westerstede Westerstede
Greece University General Hospital of Alexandroupolis Alexandroupolis
Greece Athens Medical Center-Psychikon branch Athens
Greece Henry Dunant Hospital Athens
Greece University General Hospital of Patras Patra
Greece AHEPA University General Hospital of Thessaloniki Thessaloniki
Ireland Mater Misericordiae University Hospital Dublin
Ireland Saint James's Hospital Dublin
Ireland Midland Regional Hospital - Mullingar Mullingar
Italy Ospedali Riuniti di Ancona, Clinica Ematologica Ancona
Italy Ospedale Mazzoni Ascoli Piceno
Italy Azienda Ospedaliera Policlinico di Bari Bari
Italy Monsignor Raffaele Dimiccoli Hospital Barletta
Italy Azienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia Brescia
Italy Azienda Ospedaliera di Rilievo Nazionale e di Alta Specializzazione Garibaldi Catania
Italy Azienda Ospedaliero Universitaria Policlinico Vittorio Emanuele Catania
Italy Ospedale di Civitanova Marche Civitanova Marche
Italy Azienda Ospedaliero - Universitaria Careggi Florence
Italy Presidio Ospedaliero di Livorno Livorno
Italy Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori Meldola
Italy Fondazione IRCCS Cà Grande Ospedale Maggiore Policlinico Milano
Italy Fondazione IRCCS Istituto Nazionale dei Tumori Milano
Italy Istituto Scientifico Universitario San Raffaele Milano
Italy Azienda Ospedaliera Universitaria Maggiore Della Carita di Novara Novara
Italy Fondazione IRCCS Policlinico San Matteo Pavia
Italy Azienda Ospedaliera di Perugia Perugia
Italy Azienda Ospedaliera Ospedali Riuniti Marche Nord Pesaro
Italy Azienda Unità Sanitaria Locale di Piacenza-Ospedale Guglielmo da Saliceto Piacenza
Italy Azienda Unita Sanitaria Locale di Ravenna Ravenna
Italy Arcispedale Santa Maria Nuova Reggio Emilia
Italy IRCCS Centro di Riferimento Oncologico di Basilicata di Rionero in Vulture Rionero in Vulture
Italy Istituti di Ricovero e Cura A Carattere Scientifico - Istituti Fisioterapici Ospitalieri Roma
Italy Universita degli Studi di Roma La Sapienza Roma
Italy Ospedale Casa Sollievo della Sofferenza San Giovanni Rotondo
Italy Azienda Ospedaliera Universitaria Senese-L'ospedale Santa Maria alle Scotte Siena
Italy Ospedale San Bortolo di Vicenza Vicenza
Portugal Instituto Português de Oncologia Francisco Gentil, Centro Regional de Lisboa SA Lisbon
Spain Hospital General Universitario de Alicante Alicante
Spain Hospital Universitari Germans Trias i Pujol Badalona
Spain Fundació Hospital de la Santa Creu i Sant Pau Barcelona Cataluña
Spain Hospital Universitari Mútua Terrassa Barcelona
Spain Hospital Universitario de Burgos Burgos
Spain Hospital De Cabuenes Gijon
Spain Hospital Universitario Donostia Gipuzkoa
Spain Institut Català d'Oncologia L'Hospitalet de LLobregat
Spain Hospital Universitario Severo Ochoa Leganés
Spain Hospital General Universitario Gregorio Maranon Madrid
Spain Hospital San Pedro de Alcantara Madrid
Spain Hospital Universitario Fundacion Jimenez Diaz Madrid
Spain Hospital Universitario Infanta Leonor Madrid
Spain Hospital Universitario Ramon Y Cajal Madrid
Spain Hospital Universitario Rey Juan Carlos Móstoles
Spain Hospital General Universitario Morales Meseguer Murcia
Spain Hospital Universitario Virgen de la Arrixaca Murcia
Spain Hospital Universitario Central de Asturias Oviedo
Spain Hospital Universitario Son Dureta Palma de Mallorca
Spain Clínica Universidad de Navarra Pamplona
Spain Hospital Universitario de Salamanca Salamanca
Spain Hospital Universitario de Canarias Santa Cruz de Tenerife
Spain Hospital Universitari Arnau De Vilanova (Huav) Valencia
Spain Hospital Clinico Universitario Lozano Blesa Zaragoza
Spain Hospital de Día Quirónsalud Zaragoza Zaragoza
Sweden Karolinska Universitetssjukhuset Stockholm
United Kingdom Velindre NHS Trust Cardiff
United Kingdom St George's Healthcare NHS Trust London
United Kingdom South Tees Hospitals Nhs Foundation Trust Middlesbrough
United Kingdom Abertawe Bro Morgannwg University Health Board Swansea

Sponsors (1)

Lead Sponsor Collaborator
Gilead Sciences

Countries where clinical trial is conducted

Belgium,  France,  Germany,  Greece,  Ireland,  Italy,  Portugal,  Spain,  Sweden,  United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Overall Safety Profile of Idelalisib as Measured by the Incidence of Adverse Events (AE), Serious AEs, Special Situation Reports, Adverse Drug Reactions (ADR), and Serious ADRs 250 patient-years (8 months of treatment period, 3 years of retrospective time frame, and 2.5 years of prospective observation period)
Secondary Overall Response Rate (ORR) ORR is defined as the proportion of participants who achieve a clinical response with or without radiological confirmation as documented within their electronic health record after the initiation of treatment with idelalisib and during the treatment period with idelalisib. 250 patient-years (8 months of treatment period, 3 years of retrospective time frame, and 2.5 years of prospective observation period)
Secondary Duration of Response (DOR) DOR is defined as the interval from the first documentation of a clinical response with or without radiological confirmation to the earlier of the first documentation of disease progression or death from any cause. 250 patient-years (8 months of treatment period, 3 years of retrospective time frame, and 2.5 years of prospective observation period)
Secondary Progression-free Survival (PFS) PFS is defined as the interval from the date of initiation of idelalisib to the earlier date of the first documentation of disease progression or death from any cause. 250 patient-years (8 months of treatment period, 3 years of retrospective time frame, and 2.5 years of prospective observation period)
Secondary Time to Next Treatment (TTNT) TTNT is defined as the interval from the initiation of treatment with idelalisib to the earlier date of the initiation of next systemic treatment of Follicular Lymphoma (excluding palliative care or palliative radiation) or death from any cause. 250 patient-years (8 months of treatment period, 3 years of retrospective time frame, and 2.5 years of prospective observation period)
Secondary Overall Survival (OS) OS is defined as the interval from the date of initiation of idelalisib to death from any cause. 250 patient-years (8 months of treatment period, 3 years of retrospective time frame, and 2.5 years of prospective observation period)

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