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Trial Agents

Synexus Polska Sp. z o.o

Synexus Polska Sp. z o.o is recorded as a service provider in 4 clinical trials. Explore its recorded services, study phases and therapeutic areas, with trial-level operational learnings where available.

4distinct trials
3recorded service labels
0trials with learnings

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

Clinical trial experience

Showing 4 of 4 trials · Latest update first

Master Protocol Full Title: A Master Protocol for an Exploratory, Phase 2a, Proof-of-Concept Platform Study to Evaluate the Safety, Tolerability, and Efficacy of Multiple Regimens in Participants With Myasthenia Gravis. ISA 1 Full Title: An ISA to Master Protocol ARGX-999-2-MG-2000 for an Exploratory, Phase 2a, Proof-of-Concept Study to Evaluate the Safety, Tolerability, and Efficacy of Empasiprubart IV as Add-On Therapy to Efgartigimod IV in Participants With AChR-Ab Seropositive Generalized Myasthenia Gravis With a Partial Clinical Response to Efgartigimod.

Sponsor Argenx

Start (EU)
Latest update
Estimated end

Master Protocol Full Title- A Master Protocol for an Exploratory, Phase 2a, Proof-of-Concept Platform Study to Evaluate the Safety, Tolerability, and Efficacy of Multiple Regimens in Participants With Myasthenia Gravis. ISA 2 to Master Protocol ARGX-999-2-MG-2000 – an Exploratory, Phase 2a, Randomized, Double-Blinded, Placebo-Controlled Study to Evaluate the Safety, Tolerability, and Efficacy of Empasiprubart IV Monotherapy in Participants With AChR-Ab Seropositive Generalized Myasthenia Gravis

Sponsor Argenx

Start (EU)
Latest update
Estimated end

Questions about this trial experience

What services are recorded for Synexus Polska Sp. z o.o?

The 2026-10-09 snapshot links Synexus Polska Sp. z o.o to 4 distinct CTIS trials. Recorded services include PPD Home care Service, Home Trial Services, Patient recruitment. These are study-specific roles, not a complete or independently verified capability catalogue.

Which therapeutic areas and study phases are recorded for Synexus Polska Sp. z o.o?

The most frequently recorded therapeutic areas are Immunology, Neurology, Nephrology. Recorded phases include Phase 2. Use the filters to inspect the supporting studies; missing tags are not evidence of absent experience.

In which countries are trials linked to Synexus Polska Sp. z o.o conducted?

The linked trials record locations in 13 countries, including Poland, Belgium, Spain, Italy, Germany. These are trial locations, not confirmed office locations or countries where Synexus Polska Sp. z o.o delivered services.

What can this page tell me about Synexus Polska Sp. z o.o's trial experience?

Browse 4 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 Synexus Polska Sp. z o.o. Legacy brands remain separate unless explicitly matched in the name registry.

View recorded company names
  • Synexus Polska Sp. z o.o.

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