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The Phenion® Full-Thickness Skin Model for Percutaneous Absorption Testing

Skin pharmacology and physiology, 2010-01, Vol.23 (2), p.105-112

2010

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Lipid nanoparticles for skin penetration enhancement—correlation to drug localization within the particle matrix as determined by fluorescence and parelectric spectroscopy

Journal of controlled release, 2005-12, Vol.110 (1), p.151-163

2005

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In vitro skin absorption and drug release – A comparison of six commercial prednicarbate preparations for topical use

European journal of pharmaceutics and biopharmaceutics, 2008-02, Vol.68 (2), p.380-389

2008

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Design and Evaluation of Buccal Adhesive Hydrocortisone Acetate (HCA) Tablets

Drug delivery, 2001-07, Vol.8 (3), p.161-171

2001

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Development of a Mucoadhesive Dosage Form for Vaginal Administration

Drug development and industrial pharmacy, 2001-01, Vol.27 (6), p.541-547

2001

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Correlation Between the Transdermal Permeation of Ketoprofen and its Solubility in Mixtures of a pH 6.5 Phosphate Buffer and Various Solvents

Drug delivery, 2002, Vol.9 (1), p.39-45

2002

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Mucoadhesive Tablets for Buccal Administration Containing Sodium Nimesulide

Drug delivery, 2004-01, Vol.11 (4), p.225-230

2004

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Design and in vitro-in vivo evaluation of a bi-layered tablet containing benzocaine for local buccal administration

Journal of drug delivery science and technology, 2004, Vol.14 (5), p.363-372

2004

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In vitro permeation through porcine buccal mucosa of caffeic acid phenetyl ester (CAPE) from a topical mucoadhesive gel containing propolis

Fitoterapia, 2002-11, Vol.73, p.S44-S52

2002

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NMS-P088, a CSF-1R, FLT3 and KIT inhibitor with outstanding activity on gatekeeper resistance mutations, high tolerability, and potential for combination therapies

European journal of cancer (1990), 2016-12, Vol.69, p.S127-S128

2016

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Crystal Structures of Anaplastic Lymphoma Kinase in Complex with ATP Competitive Inhibitors

Biochemistry (Easton), 2010-08, Vol.49 (32), p.6813-6825

2010

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NMS-173, a potent, covalent second generation IDH1/IDH2 inhibitor

European journal of cancer (1990), 2022-10, Vol.174, p.S17-S17

2022

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Abstract 1324: NMS-P088, a novel FLT3, KIT and CSF1R inhibitor, is a promising clinical candidate for AML and CMML treatment

Cancer research (Chicago, Ill.), 2019-07, Vol.79 (13_Supplement), p.1324-1324

2019

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A Phase I/II Study of NMS-03592088, a FLT3, KIT and CSF1R Inhibitor, in Patients with Relapsed or Refractory AML or CMML

Blood, 2019-11, Vol.134 (Supplement_1), p.3855-3855

2019

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Abstract 805: NMS-P088, a FLT3-KIT-CSF-1R inhibitor with activity on FLT3 F691L as a novel agent in AML

Cancer research (Chicago, Ill.), 2018-07, Vol.78 (13_Supplement), p.805-805

2018

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Abstract 4785: NMS-E668, a highly potent orally available RET inhibitor with selectivity towards VEGFR2 and demonstrated antitumor efficacy in multiple RET-driven cancer models

Cancer research (Chicago, Ill.), 2018-07, Vol.78 (13_Supplement), p.4785-4785

2018

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Italian survey about intraperitoneal drain use in distal pancreatectomy

Updates in surgery, 2024-10

2024

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Multistep synthesis of a new tricyclic azaindole-based scaffold

Tetrahedron letters, 2009-09, Vol.50 (36), p.5156-5158

2009

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Correction: Intraperitoneal prophylactic drain after pancreaticoduodenectomy: an Italian survey

Updates in surgery, 2024-10, Vol.76 (6), p.2501-2501

2024

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Intraperitoneal prophylactic drain after pancreaticoduodenectomy: an Italian survey

Updates in surgery, 2024-06, Vol.76 (3), p.923-932

2024

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Abstract 798: NMS-P088, a dual FLT3-KIT inhibitor active also on gatekeeper mutations and devoid of QTc prolongation

Cancer research (Chicago, Ill.), 2015-08, Vol.75 (15_Supplement), p.798-798

2015

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388 - NMS-P088, a CSF-1R, FLT3 and KIT inhibitor with outstanding activity on gatekeeper resistance mutations, high tolerability, and potential for combination therapies

European journal of cancer (1990), 2016-12, Vol.69, p.S127-S128

2016

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The Phenion® Full-Thickness Skin Model for Percutaneous Absorption Testing

Lipid nanoparticles for skin penetration enhancement—correlation to drug localization within the particle matrix as determined by fluorescence and parelectric spectroscopy

In vitro skin absorption and drug release – A comparison of six commercial prednicarbate preparations for topical use

Design and Evaluation of Buccal Adhesive Hydrocortisone Acetate (HCA) Tablets

Development of a Mucoadhesive Dosage Form for Vaginal Administration

Correlation Between the Transdermal Permeation of Ketoprofen and its Solubility in Mixtures of a pH 6.5 Phosphate Buffer and Various Solvents

Mucoadhesive Tablets for Buccal Administration Containing Sodium Nimesulide

Design and in vitro-in vivo evaluation of a bi-layered tablet containing benzocaine for local buccal administration

In vitro permeation through porcine buccal mucosa of caffeic acid phenetyl ester (CAPE) from a topical mucoadhesive gel containing propolis

Discovery of Entrectinib: A New 3‑Aminoindazole As a Potent Anaplastic Lymphoma Kinase (ALK), c‑ros Oncogene 1 Kinase (ROS1), and Pan-Tropomyosin Receptor Kinases (Pan-TRKs) inhibitor

The TPM3-NTRK1 rearrangement is a recurring event in colorectal carcinoma and is associated with tumor sensitivity to TRKA kinase inhibition

NMS-P088, a CSF-1R, FLT3 and KIT inhibitor with outstanding activity on gatekeeper resistance mutations, high tolerability, and potential for combination therapies

Crystal Structures of Anaplastic Lymphoma Kinase in Complex with ATP Competitive Inhibitors

NMS-173, a potent, covalent second generation IDH1/IDH2 inhibitor

Abstract 1324: NMS-P088, a novel FLT3, KIT and CSF1R inhibitor, is a promising clinical candidate for AML and CMML treatment

A Phase I/II Study of NMS-03592088, a FLT3, KIT and CSF1R Inhibitor, in Patients with Relapsed or Refractory AML or CMML

Abstract 805: NMS-P088, a FLT3-KIT-CSF-1R inhibitor with activity on FLT3 F691L as a novel agent in AML

Abstract 4785: NMS-E668, a highly potent orally available RET inhibitor with selectivity towards VEGFR2 and demonstrated antitumor efficacy in multiple RET-driven cancer models

Correction to Discovery of Entrectinib: A New 3‑Aminoindazole as a Potent Anaplastic Lymphoma Kinase (ALK), c‑ros Oncogene 1 Kinase (ROS1), and Pan-Tropomyosin Receptor Kinases (Pan-TRKs) inhibitor

Italian survey about intraperitoneal drain use in distal pancreatectomy

Multistep synthesis of a new tricyclic azaindole-based scaffold

Correction: Intraperitoneal prophylactic drain after pancreaticoduodenectomy: an Italian survey

Intraperitoneal prophylactic drain after pancreaticoduodenectomy: an Italian survey

Abstract 798: NMS-P088, a dual FLT3-KIT inhibitor active also on gatekeeper mutations and devoid of QTc prolongation

388 - NMS-P088, a CSF-1R, FLT3 and KIT inhibitor with outstanding activity on gatekeeper resistance mutations, high tolerability, and potential for combination therapies

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