Consorzio Per Valutazioni Biologiche E Farmacologiche
Consorzio Per Valutazioni Biologiche E Farmacologiche is recorded as a service provider in 18 clinical trials. Explore its recorded services, study phases and therapeutic areas, with trial-level operational learnings where available.
Clinical trial experience
Showing 18 of 18 trials · Latest update first
A Single-arm, Phase II Study to Evaluate the Efficacy and Safety of Linperlisib (YY-20394) Monotherapy in Patients with Relapsed or Refractory Peripheral T/NK Cell or Cutaneous T Cell Lymphoma
Sponsor Shanghai Yingli Pharmaceutical Co. Ltd.
- Start (EU)
- Latest update
- Estimated end
Operational learnings available5 trial-level findings · Read insights
- The trial enrolled 45 of approximately 107 planned participants at 6 sites in the United States and Italy, and Stage 2 of the Simon two-stage design was not conducted.
- The protocol specified independent radiology review for the primary endpoint, but no independent radiology review was performed and response results were investigator assessed.
- Thirty-eight participants (84.4%) had at least one important protocol deviation, most commonly safety-assessment deviations (73.3%) and visit-window deviations (24.4%).
- End-of-study data were not recorded for 1 participant because the site closed.
- The exploratory CTCL cohort enrolled 10 participants, and disease stage at initial diagnosis was missing for 8 of them.
These findings describe the trial, not the service provider’s performance or responsibility.
Neurodevelopmental outcome after standard dose sevoflurane versus low-dose sevoflurane/dexmedetomidine/remifentanil anaesthesia in young children
Sponsor Giannina Gaslini Institute For Scientific Hospitalization And Care
- Start (EU)
- Latest update
- Estimated end
Head-to-head comparison of single versus dual antiplatelet treatment strategy after percutaneous left atrial appendage closure: A multicenter, randomized study. The ARMYDA-AMULET study
Sponsor Fondazione Toscana Gabriele Monasterio
- Start (EU)
- Latest update
- Estimated end
- Not reported
Early oral step-down antibiotic therapy versus continuing intravenous therapy for uncomplicated Gram-negative bacteraemia (the INVEST trial)
Sponsor Tan Tock Seng Hospital Pte. Ltd.
- Start (EU)
- Latest update
- Estimated end
LBL 2018 – International cooperative treatment protocol for children and adolescents with lymphoblastic lymphoma
Sponsor Universitaetsklinikum Muenster AöR
- Start (EU)
- Latest update
- Estimated end
EaRly impAct theraPy with ceftazidime-avibactam via rapID diagnostics versus standard of care antibiotics and diagnostics in patients with bloodstream infection, hospital-acquired pneumonia or ventilator-associated pneumonia due to Pseudomonas aeruginosa or carbapenemase producing Enterobacterales (“RAPID”)
Sponsor National University Of Singapore
- Start (EU)
- Not reported
- Latest update
- Estimated end
Low dose TamOxifen and LifestylE changes for bReast cANcer prevenTion: a randomized phase II biomarker trial in subjects at increased risk (TOLERANT Study)
Sponsor Istituto Europeo Di Oncologia S.r.l.
- Start (EU)
- Latest update
- Estimated end
- Not reported
Repurposing mirtazapine in Rett syndrome: a multicentric open label Phase II study (MirtaRett Study).
Sponsor University Of Trieste
- Start (EU)
- Latest update
- Estimated end
- Not reported
An Italian multicenter phase II trial of Metronomic Temozolomide in unfit patients with advanced neuroendocrine neoplasms (NENs): MeTe study
Sponsor Istituto Europeo Di Oncologia S.r.l.
- Start (EU)
- Latest update
- Estimated end
- Not reported
Elacestrant and exemestane for patients with pretreated HR+/HER2- metastatic breast cancer and [18F]-FES-avid lesions (COMBINE): a proof-of-concept phase 2 clinical trial
Sponsor Istituto Europeo Di Oncologia S.r.l.
- Start (EU)
- Latest update
- Estimated end
- Not reported
Combination of pembrolizumab with oral metronomic cyclophosphamide in patients with chest wall breast cancer (PERICLES): A phase II study
Sponsor Istituto Europeo Di Oncologia S.r.l.
- Start (EU)
- Latest update
- Estimated end
- Not reported
Phase I single arm, dose escalating and phase II double blind, randomized, placebo-controlled dose finding clinical trial assessing safety, and efficacy of intratracheal administration of allogeneic umbilical mesenchymal cells-derived extracellular vesicles in preventing bronchopulmonary dysplasia in extremely preterm newborns.
Sponsor Exo Biologics
- Start (EU)
- Latest update
- Estimated end
- Not reported
A phase III, randomized, double blind, multiple doses, placebo-controlled parallel-group, adaptive study to evaluate the efficacy of atropine to treat the progression of myopia in children and adolescents from 3 to less than 18 years of age (MODERATO Study)
Sponsor Ocus Innovation Ireland Limited
- Start (EU)
- Latest update
- Estimated end
PROPOSE: Effect of Intravaginal Prasterone on Genitourinary Syndrome in Women in Menopause with previous Breast Cancer or currently under treatment with endocrine therapy for Breast Cancer with aromatase inhibitor +/- LHRHa
Sponsor Istituto Europeo Di Oncologia S.r.l.
- Start (EU)
- Latest update
- Estimated end
- Not reported
AZALEA: A Phase II study of atezolizumab, vinorelbine and weekly cyclophosphamide as T-cell activators in first line metastatic triple negative breast cancer patients pre-treated with anti-PD-L1/PD-1
Sponsor Istituto Europeo Di Oncologia S.r.l.
- Start (EU)
- Latest update
- Estimated end
- Not reported
Randomized, multicenter, open-label study on PREvention of respiratory SEquelae of RSV bronchiolitis in preterm babies (PRESERV)
Sponsor Azienda Sanitaria Locale Della Provincia Di Biella
- Start (EU)
- Latest update
- Estimated end
- Not reported
Efficacy and safety of memantine as antimanic and mood-stabilizing medication for adolescents with Bipolar Disorder: a monocentric, randomized, double-blind, placebo-controlled clinical trial.
Sponsor Ospedale Pediatrico Bambino Gesu
- Start (EU)
- Latest update
- Estimated end
- Not reported
Statin Effect on ARrhythmogenic CardiomyopatHy disease progression
Sponsor Centro Cardiologico Monzino S.p.A.
- Start (EU)
- Latest update
- Estimated end
- Not reported
Questions about this trial experience
What services are recorded for Consorzio Per Valutazioni Biologiche E Farmacologiche?
The 2026-10-09 snapshot links Consorzio Per Valutazioni Biologiche E Farmacologiche to 18 distinct CTIS trials. Recorded services include Safety reporting & pharmacovigilance, Clinical monitoring, Regulatory services, Project management, among 13 recorded service labels. These are study-specific roles, not a complete or independently verified capability catalogue.
Which therapeutic areas and study phases are recorded for Consorzio Per Valutazioni Biologiche E Farmacologiche?
The most frequently recorded therapeutic areas are Haematological Malignancies, Infectious Disease, Cardiology, Dermatology. Recorded phases include Phase 4, Phase 2, Phase 3. Use the filters to inspect the supporting studies; missing tags are not evidence of absent experience.
In which countries are trials linked to Consorzio Per Valutazioni Biologiche E Farmacologiche conducted?
The linked trials record locations in 15 countries, including Italy, Spain, Belgium, Greece, Poland. These are trial locations, not confirmed office locations or countries where Consorzio Per Valutazioni Biologiche E Farmacologiche delivered services.
What can this page tell me about Consorzio Per Valutazioni Biologiche E Farmacologiche's trial experience?
Browse 18 distinct trials with recorded roles, sponsor names, available study dates and links to CTIS source records. 1 trials have operational findings that can inform further due diligence. Trial counts and findings do not measure the provider’s performance or establish responsibility for study outcomes.
About this data & company names
One current approved profile per CTIS trial. Services reflect recorded roles, not a complete capability catalogue or a performance ranking. Missing tags mean the information was not recorded. Country tags describe trial locations, not the provider’s service territory.
Start is the reported EU start date; latest update is the CTIS publication date; estimated end is the reported global estimate, which may be in the past. Missing dates are shown as “Not reported”. Operational learnings describe the trial as a whole and do not establish the provider’s responsibility.
Clear service synonyms are grouped; otherwise the source label is retained. Service tags show the recorded roles for each trial. This page groups 1 recorded name variant under Consorzio Per Valutazioni Biologiche E Farmacologiche. Legacy brands remain separate unless explicitly matched in the name registry.
View recorded company names
- Consorzio Per Valutazioni Biologiche E Farmacologiche