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A Study to Asses Effectiveness and Treatment Management of Oral Venetoclax Tablets + Subcutaneously Injected Azacitidine in Adult Participants Ineligible for Intensive Chemotherapy With de Novo Acute Myeloid Leukemia (AML) in Italy

Active, not recruiting
Conditions
Acute Myeloid Leukemia
Registration Number
NCT06058741
Lead Sponsor
AbbVie
Brief Summary

Acute myeloid leukemia (AML) is a cancer of the blood and bone marrow and is the most common acute leukemia in adults. This study will evaluate how well venetoclax in combination with azacitidine works to treat AML in newly diagnosed adult participants who are ineligible for intensive chemotherapy in Italy.

Venetoclax in combination with azacitidine is approved in Italy to treat Acute myeloid leukemia (AML) in newly diagnosed adults who are ineligible for intensive chemotherapy. All study participants will receive venetoclax in combination with azacitidine as prescribed by their study doctor in accordance with approved local label. Adult participants with a new diagnosis of AML will be enrolled. Around 150 participants will be enrolled in the study at approximately 20-25 sites in Italy.

Participants will receive venetoclax tablets to be taken by mouth in combination with azacitidine given by subcutaneous (SC) injection according to the approved local label. The duration of the study is approximately 18 months.

There is expected to be no additional burden for participants in this trial. All study visits will occur during routine clinical practice and participants will be followed for 18 months.

Detailed Description

Not available

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
150
Inclusion Criteria
  • Confirmed diagnosis of primary or secondary acute myeloid leukemia (AML), deemed ineligible for intensive induction chemotherapy because of age, performance status, comorbidities or any other clinical reason as defined by the treating physician.
  • Investigator decision on patient treatment with venetoclax + azacitidine must have been reached prior to and independently of recruitment in the study.
  • Treatment prescribed in accordance with the applicable approved label and local regulatory and reimbursement policies.
Exclusion Criteria
  • Participants affected by Acute Promyelocytic Leukemia.
  • Prior treatment for AML, excluding hydroxyurea.
  • Participation in a clinical trial of an investigational drug, concurrently or within the last 30 days. Participation in another post-marketing observational study or Registry is acceptable

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Overall Survival (OS)Up to 18 Months

OS is defined as time from treatment initiation to death from any cause.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (28)

Azienda Ospedaliero Universitaria delle Marche /ID# 261822

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Ancona, Italy

Ospedale San Martino /ID# 258981

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Genoa, Genova, Italy

IRCCS Istituto Clinico Humanitas /ID# 259300

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Rozzano, Lombardia, Italy

AST Pesaro Urbino /ID# 261400

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Pesaro, Marche, Italy

ASST Valle Olona/Ospedale di Busto Arsizio /ID# 259833

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Busto Arsizio, Milano, Italy

ASST Grande Ospedale Metropolitano Niguarda /ID# 259455

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Milan, Milano, Italy

Azienda Ospedaliera di Rilievo Nazionale Antonio Cardarelli /ID# 261794

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Naples, Napoli, Italy

AOU Policlinico G. Rodolico - San Marco /ID# 261223

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Catania, Italy

A.O.U. CITTA' DELLA SALUTE E DELLA SCIENZA DI TORINO - Ospedale Molinette /ID# 258720

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Torino, Piemonte, Italy

Istituto Romagnolo per lo Studio dei Tumori Dino Amadori IRST - IRCCS /ID# 260963

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Meldola, Reggio Emilia, Italy

Azienda Ospedaliera Universitaria Policlinico Tor Vergata /ID# 260683

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Rome, Roma, Italy

Azienda Ospedaliero-Universitaria Policlinico Umberto I /ID# 260821

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Rome, Roma, Italy

Presidio Ospedaliero Vito Fazzi /ID# 261222

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Lecce, Puglia, Italy

Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico /ID# 260738

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Milano, Italy

Azienda Ospedaliero-Universitaria di Modena /ID# 259189

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Modena, Italy

IRCCS AOU di Bologna Policlinico Sant Orsola Malpighi /ID# 259535

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Bologna, Italy

ASST Papa Giovanni XXIII /ID# 258727

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Bergamo, Italy

Azienda Ospedaliera Universitaria Integrata di Verona /ID# 260809

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Verona, Italy

Azienda Ospedaliero Universitaria Careggi /ID# 259766

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Florence, Firenze, Italy

Azienda Ospedaliero Universitaria Maggiore della Carita di Novara /ID# 259778

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Novara, Italy

Fondazione IRCCS Policlinico San Matteo /ID# 259624

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Pavia, Italy

Azienda Ospedaliera di Perugia - Ospedale S. Maria della Misericordia /ID# 258983

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Perugia, Italy

Azienda Ospedaliera Ospedali Riuniti Villa Sofia Cervello /ID# 261146

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Palermo, Italy

Azienda Sanitaria Locale Pescara-Presidio Ospedaliero S.Spirito /ID# 261304

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Pescara, Italy

Grande Ospedale Metropolitano Bianchi - Melacrino - Morelli P.O. Riuniti /ID# 260737

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Reggio Calabria, Italy

AOU San Giovanni di Dio Ruggi d'Aragona - Scuola Medica Salernitana /ID# 259456

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Salerno, Italy

Azienda Sanitaria Universitaria Giuliano Isontina /ID# 261298

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Trieste, Italy

Ospedale Belcolle /ID# 259563

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Viterbo, Italy

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