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Trial Agents

LYSARC

LYSARC is recorded as a service provider in 6 clinical trials. Explore its recorded services, study phases and therapeutic areas, with trial-level operational learnings where available.

6distinct trials
7recorded service labels
0trials with learnings

Data snapshot: 2026-10-09 · About the data

Clinical trial experience

Showing 6 of 6 trials · Latest update first

A phase 3 multicenter, randomised, prospective, open-label trial of fixed-duration (12 cycles) venetoclax/ obinutuzumab vs. fixed-duration (15 cycles) venetoclax/ pirtobrutinib vs. MRD-guided venetoclax/ pirtobrutinib in patients with previously untreated chronic lymphocytic leukaemia (CLL)/ small lymphocytic lymphoma (SLL) aiming to establish measurement of individual residual disease for adjustment of treatment duration to improve outcomes (CLL18/MOIRAI)

Sponsor University Of Cologne

Start (EU)
Latest update
Estimated end

A PHASE III, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED TRIAL COMPARING THE EFFICACY AND SAFETY OF POLATUZUMAB VEDOTIN IN COMBINATION WITH RITUXIMAB AND CHP (R-CHP) VERSUS RITUXIMAB AND CHOP (R-CHOP) IN PREVIOUSLY UNTREATED PATIENTS WITH DIFFUSE LARGE B-CELL LYMPHOMA

Sponsor F. Hoffmann-La Roche AG

Start (EU)
Latest update
Estimated end

MALIBU trial - Phase II study of combination ibrutinib and rituximab in untreated marginal zone lymphomas

Sponsor Association International Extranodal Lymphoma Study Group (IELSG)

Start (EU)
Latest update
Estimated end

Questions about this trial experience

What services are recorded for LYSARC?

The 2026-10-09 snapshot links LYSARC to 6 distinct CTIS trials. Recorded services include Clinical monitoring, Regulatory services, Investigator recruitment, centralized anatomopathologocal review (LYSA-P) and for SMZL patients a cytological review at LYON, among 7 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 LYSARC?

The most frequently recorded therapeutic areas are Haematological Malignancies. Recorded phases include 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 LYSARC conducted?

The linked trials record locations in 15 countries, including France, Italy, Belgium, Germany, Poland. These are trial locations, not confirmed office locations or countries where LYSARC delivered services.

What can this page tell me about LYSARC's trial experience?

Browse 6 distinct trials with recorded roles, sponsor names, available study dates and links to CTIS source records. No trial-level operational findings are recorded in this snapshot. 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 LYSARC. Legacy brands remain separate unless explicitly matched in the name registry.

View recorded company names
  • LYSARC

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