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Trial Agents

Hematogenix

Hematogenix is recorded as a service provider in 7 clinical trials. Explore its recorded services, study phases and therapeutic areas, with trial-level operational learnings where available.

7distinct trials
4recorded service labels
1trials with learnings

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

Clinical trial experience

Showing 7 of 7 trials · Latest update first

A Phase 3 Randomized, Double-blind, Placebo-controlled, Study of Bleximenib, Venetoclax and Azacitidine for the Treatment of Participants with Newly Diagnosed Acute Myeloid Leukemia Harboring KMT2ARearrangements or NPM1Mutations who are Ineligible for Intensive Chemotherapy

Sponsor Janssen Cilag International

Start (EU)
Latest update
Estimated end

A Phase 3 Randomized Study Comparing Talquetamab SC in Combination With Daratumumab SC and Pomalidomide (Tal-DP) or Talquetamab SC in Combination With Daratumumab SC (Tal-D) Versus Daratumumab SC, Pomalidomide and Dexamethasone (DPd), in Participants With Relapsed or Refractory Multiple Myeloma who Have Received at Least 1 Prior Line of Therapy

Sponsor Janssen - Cilag International

Start (EU)
Latest update
Estimated end

A Phase 3, Randomized, Multicenter, Open-label Study to Evaluate the Efficacy and Safety of Alnuctamab Compared to Standard of Care Regimens in Participants with Relapsed or Refractory Multiple Myeloma (RRMM) - ALUMMINATE RRMM

Sponsor Not reported

Start (EU)
Not reported
Latest update
Estimated end
Operational learnings available1 trial-level finding · Read insights
  • The trial was withdrawn with 0 patients enrolled.

These findings describe the trial, not the service provider’s performance or responsibility.

A Phase 3 Randomized Study Comparing Teclistamab in Combination with Daratumumab SC (Tec-Dara) versus Daratumumab SC, Pomalidomide, and Dexamethasone (DPd) or Daratumumab SC, Bortezomib, and Dexamethasone (DVd) in Participants with Relapsed or Refractory Multiple Myeloma

Sponsor Janssen - Cilag International

Start (EU)
Latest update
Estimated end

A Phase 3, Two-Stage, Randomized, Multicenter, Open-label Study Comparing Iberdomide, Daratumumab and Dexamethasone (IberDd) versus Daratumumab, Bortezomib, and Dexamethasone (DVd) in Subjects with Relapsed or Refractory Multiple Myeloma (RRMM) (EXCALIBER-RRMM)

Sponsor Celgene Corp.

Start (EU)
Latest update
Estimated end

Questions about this trial experience

What services are recorded for Hematogenix?

The 2026-10-09 snapshot links Hematogenix to 7 distinct CTIS trials. Recorded services include Laboratory services, Lab kits and collection services for PD samples, Logistic Support of samples, kit management, Flow Cytometry, Morphological Assessment, Primary/ surrogate endpoint test, kit build, sample management, and result management for BMA MRD (via NGF assay) samples. These are study-specific roles, not a complete or independently verified capability catalogue.

Which therapeutic areas and study phases are recorded for Hematogenix?

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

The linked trials record locations in 18 countries, including Spain, France, Belgium, Germany, Italy. These are trial locations, not confirmed office locations or countries where Hematogenix delivered services.

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

Browse 7 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 Hematogenix. Legacy brands remain separate unless explicitly matched in the name registry.

View recorded company names
  • Hematogenix

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