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Trial Agents

Acetaminophen Toxicity Diagnostics

Acetaminophen Toxicity Diagnostics is recorded as a service provider in 16 clinical trials. Explore its recorded services, study phases and therapeutic areas, with trial-level operational learnings where available.

16distinct trials
3recorded service labels
0trials with learnings

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

Clinical trial experience

Showing 16 of 16 trials · Latest update first

A Phase 3, Randomized, Multicenter, Open-Label Study of Velzatinib (GSK6042981) versus Imatinib in Participants with Previously Untreated Metastatic and/or Unresectable Gastrointestinal Stromal Tumors (GIST)

Sponsor Glaxosmithkline Research & Development Limited

Start (EU)
Latest update
Estimated end

A Phase 3, Randomized, Double-Blind, Placebo-Controlled, 3-Arm Study to Investigate the Safety and Efficacy of Efimosfermin Alfa in Participants With Biopsy-Confirmed F2- or F3-Stage Metabolic Dysfunction-Associated Steatohepatitis (MASH) (ZENITH-1)

Sponsor Glaxosmithkline Research & Development Limited

Start (EU)
Latest update
Estimated end

A randomized, open-label, multicenter, Phase 3 study to investigate mocertatug rezetecan compared with chemotherapy in participants with endometrial cancer after platinum-based chemotherapy and immunotherapy

Sponsor Glaxosmithkline Research & Development Limited

Start (EU)
Not reported
Latest update
Estimated end

A Phase III, Multicenter, Open-Label, Randomized Study to Evaluate the Efficacy and Safety of Belantamab Mafodotin in Combination with Pomalidomide and Dexamethasone (B-Pd) versus Pomalidomide plus Bortezomib and Dexamethasone (PVd) in Participants with Relapsed/Refractory Multiple Myeloma (DREAMM 8)

Sponsor Glaxosmithkline Research & Development Limited

Start (EU)
Latest update
Estimated end

A Phase 3, Randomized, Double-Blind, Placebo-Controlled, 3-Arm Study to Investigate the Safety and Tolerability of Efimosfermin Alfa in Participants With Known or Suspected F2- or F3-Stage Metabolic Dysfunction-Associated Steatohepatitis (MASH) (ZENITH-2)

Sponsor Glaxosmithkline Research & Development Limited

Start (EU)
Latest update
Estimated end

The MODIFY Study: A Phase 3b/4 randomized, double-blind, placebo-controlled, multicentre study evaluating the impact of early intervention with depemokimab on exacerbation rate, clinical remission, lung function decline, and safety in adults and adolescents with at risk Type 2 asthma, conducted up to 156 weeks.

Sponsor Glaxosmithkline Research & Development Limited

Start (EU)
Latest update
Estimated end

A 52-week, randomized, double-blind, double-dummy, parallel-group, multi-centre, non-inferiority study to investigate the efficacy and safety of depemokimab compared with mepolizumab in adults with relapsing or refractory Eosinophilic Granulomatosis with Polyangiitis (EGPA) receiving standard of care (SoC) therapy

Sponsor Glaxosmithkline Research & Development Limited

Start (EU)
Latest update
Estimated end

A Phase 3b, multicenter, single-arm, open-label study evaluating the efficacy, safety, and tolerability of switching to DTG/3TC single tablet regimen administered once daily from a bictegravir/emtricitabine/tenofovir alafenamide single tablet regimen in people living with HIV of at least 50 years of age who are virologically suppressed

Sponsor Viiv Healthcare UK Limited

Start (EU)
Latest update
Estimated end

Questions about this trial experience

What services are recorded for Acetaminophen Toxicity Diagnostics?

The 2026-10-09 snapshot links Acetaminophen Toxicity Diagnostics to 16 distinct CTIS trials. Recorded services include Laboratory services, acetaminophen testing for liver events, Analysis of Acetaminophen. These are study-specific roles, not a complete or independently verified capability catalogue.

Which therapeutic areas and study phases are recorded for Acetaminophen Toxicity Diagnostics?

The most frequently recorded therapeutic areas are Solid Tumor Oncology, Gastroenterology, Gynecology, Haematological Malignancies. Recorded phases include Phase 3, Phase 1, Phase 2, Phase 4. Use the filters to inspect the supporting studies; missing tags are not evidence of absent experience.

In which countries are trials linked to Acetaminophen Toxicity Diagnostics conducted?

The linked trials record locations in 19 countries, including Spain, France, Italy, Germany, Belgium. These are trial locations, not confirmed office locations or countries where Acetaminophen Toxicity Diagnostics delivered services.

What can this page tell me about Acetaminophen Toxicity Diagnostics's trial experience?

Browse 16 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 3 recorded name variants under Acetaminophen Toxicity Diagnostics. Legacy brands remain separate unless explicitly matched in the name registry.

View recorded company names
  • Acetaminophen Toxicity Diagnostics
  • Acetaminophen Toxicity Diagnostics LLC
  • Acetaminophen Toxicity Diagnostics, LLC

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