Rete Oncologica Piemonte e Valle d'Aosta

MULTIPATOLOGIA

ASL Alessandria

Studio TT-TOX: il triage telefonico infermieristico delle tossicità in onco-ematologia. Uno studio osservazionale multicentrico no-profit

Attività fisica in oncologia – progettazione di un percorso di attività fisica basato sulle percezioni, i vissuti e desideri dei pazienti oncologici (AFION)

ASL Biella

Studio NICSO (Network Italiano Cure di Supporto in Oncologia): “Progetto di Monitoraggio Medico – Infermieristico degli Effetti Collaterali da Terapie Oncologiche.

ASL CN1

Nutritional status and Body composition impact on gynecological patients treated with innovative cancer therapies (the MITO 50 – NOBODY cancer multicenter study)

A.O. S. Croce e Carle di Cuneo

MITO 35a: a multicenter, prospective, single arm trial of Olaparib maintenance therapy in newly diagnosed BRCA wildtype advanced ovarian, fallopian tube and primitive peritoneal cancer.

Randomized Study of Paclitaxel – Carboplatin followed by maintenance Niraparib compared to Paclitaxel – Carboplatin – Bevacizumab followed by maintenance Niraparib + Bevacizumab in Patients With Advanced Ovarian Cancer, Following a Front-Line Complete Cytoreductive Surgery

AUSL Valle d’Aosta

Individuazione delle alterazioni genomiche presenti nei pazienti affetti da malattia tumorale, nella Regione Valle d’Aosta

Humanitas Gradenigo Torino

L’impatto dei parametri immunitario-infiammatori- nutrizionali sulla prognosi dei pazienti affetti da tumore solido avanzato in trattamento con agente immunoterapico

I.N.O.C. Candiolo

CDAK539A12103 (Sponsor Novartis) A Phase 1b, Open-Label, Multicenter Study to Evaluate the Pharmacokinetic Profile of Pelabresib (DAK539/CPI-0610) in Patients with Advanced Malignancies and Hepatic Impairment

DS7300-203 (Sponsor Daiichi Sankyo, Inc): A phase 1b/2 pan-tumor, open-label study to evaluate the efficacy and safety of ifinatamab deruxtecan (i-dxd) in subjects with recurrent or metastatic solid tumors.

PYNNACLE (PMV Pharmaceuticals) A Phase 1/2 Open-label, Multicenter Study to Assess the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Efficacy of PC14586 in Patients with Locally Advanced or Metastatic Solid Tumors Harboring a TP53 Y220C Mutation

D3S-001-100 (Sponsor D3 Bio): A Phase 1, Open-label, Dose-escalation and Dose-expansion Study Evaluating the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Preliminary Efficacy of D3S-001 Monotherapy in Subjects with Advanced Solid Tumors with a KRAS p.G12C Mutation

KO-2806-001 (Sponsor Kura Oncology, Inc): Phase 1, First-in-Human, Multicenter, Open-Label Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Preliminary Antitumor Activity of KO-2806 When Administered as Monotherapy and in Combination Therapy in Adult Patients with Advanced Solid Tumors.

VALO-001 (Sponsor Valo Therapeutics) A Phase I, open-label, non-randomized study to evaluate the safety and Immune activity of PeptiCRAd-1, a tumor-specific peptide coated conditionally replicating adenovirus, in combination with immune checkpoint inhibitor pembrolizumab in patients with injectable solid tumors in indications known to express NY-ESO-1 and MAGE-A3

CA2440001 (Sponsor BMS): A Phase 1/2a, Open-label, Dose-finding Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Preliminary Efficacy of BMS-986507 (BL-B01D1) combinations in Adult Participants with Advanced Solid Tumors

A.S.L. CN2

Italian Registry on rAre genito-uRinary nEoplasms – Meet-URO 23 study (I-RARE study)

 

 

Patologia

Multipatologia
Rete Oncologica Piemonte e Valle d'Aosta
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