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Trial Agents

Abf Pharmaceutical Services

Abf Pharmaceutical Services is recorded as a service provider in 32 clinical trials. Explore its recorded services, study phases and therapeutic areas, with trial-level operational learnings where available.

32distinct trials
24recorded service labels
2trials with learnings

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

Clinical trial experience

Showing 20 of 32 trials · Latest update first

A Phase 2, Multicenter, Randomized, Double-blind, Placebo‑controlled Study with Deferred Active Treatment to Investigate the Efficacy, Safety, and Pharmacokinetics of JNJ‑73763989 + Nucleos(t)ide Analog in Participants Co‑infected with Hepatitis B and Hepatitis D Virus

Sponsor Janssen - Cilag International

Start (EU)
Latest update
Estimated end
Operational learnings available5 trial-level findings · Read insights
  • Approximately 50% of the first 22 Part 1 participants experienced on-treatment ALT elevations, and protocol management criteria were amended because some elevations were prolonged.
  • New enrollment was temporarily halted in December 2022 after significant ALT elevations were observed more frequently in Part 2 participants with screening or baseline HBsAg >10,000 IU/mL.
  • Enrollment was not reopened because the sponsor discontinued further investment in its hepatitis B and D discovery and development programs.
  • Part 2 open-label treatment was reduced to Week 96 and follow-up to 24 weeks under protocol amendment 5.
  • Sustained HBV response was not collected or analyzed because follow-up was shortened and participants continued NA treatment during follow-up.

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

An open-label, multi-center, roll-over study to assess long-term safety in subjects who are ongoing or have completed a prior global Novartis or GSK sponsored Tafinlar (dabrafenib) and/or Mekinist (trametinib) study and are judged by the investigator to benefit from continued treatment

Sponsor Novartis Pharma AG

Start (EU)
Latest update
Estimated end

An open-label Phase II/III randomized trial of BNT113 in combination with pembrolizumab versus pembrolizumab monotherapy as a first line therapy in patients with unresectable recurrent, or metastatic Head and Neck Squamous Cell Carcinoma (HNSCC) which is positive for human papilloma virus 16 (HPV16+) and expresses PD-L1

Sponsor BioNTech SE

Start (EU)
Latest update
Estimated end

A randomized, double-blind, placebo-controlled multicenter study to evaluate the effect of inclisiran on preventing major adverse cardiovascular events in high-risk primary prevention patients (VICTORION-1 PREVENT)

Sponsor Novartis Pharma AG

Start (EU)
Latest update
Estimated end

KontRASt-06: An open-label phase II trial evaluating the activity and safety of JDQ443 single-agent as first-line treatment for patients with locally advanced or metastatic KRAS G12C-mutated non-small cell lung cancer with a PD-L1 expression < 1% or a PD-L1 expression ≥ 1% and an STK11 co-mutation.

Sponsor Novartis Pharma AG

Start (EU)
Latest update
Estimated end

A 2-year randomized, 3-arm, double-blind, non-inferiority study comparing the efficacy and safety of ofatumumab and siponimod versus fingolimod in pediatric patients with multiple sclerosis followed by an open-label extension

Sponsor Novartis Pharma AG

Start (EU)
Latest update
Estimated end

An open-label, single arm, multi-center extension study evaluating long-term safety, tolerability and effectiveness of ofatumumab in subjects with relapsing multiple sclerosis (RMS)

Sponsor Novartis Pharma AG

Start (EU)
Latest update
Estimated end

A randomized, double-blind, placebo -controlled, multicenter trial, assessing the impact of inclisiran on major adverse cardiovascular events in participants with established cardiovascular disease (VICTORION-2 PREVENT)

Sponsor Novartis Pharma AG

Start (EU)
Latest update
Estimated end

A randomized, double-blind 2-arm NEPTUNUS extension study followed by an open-label single-arm study to assess the long-term safety and efficacy of ianalumab in patients with Sjögren’s syndrome

Sponsor Novartis Pharma AG

Start (EU)
Latest update
Estimated end

A randomized, subject and investigator blinded, placebo controlled and multi-center platform study, to assess efficacy and safety of different investigational drugs in patients with moderate to severe hidradenitis suppurativa

Sponsor Novartis Pharma AG

Start (EU)
Latest update
Estimated end

A randomized double-blind, placebo-controlled, multicenter trial assessing the impact of lipoprotein (a) lowering with pelacarsen (TQJ230) on major cardiovascular events in patients with established cardiovascular disease

Sponsor Novartis Pharma AG

Start (EU)
Latest update
Estimated end

Open-label, randomized Phase II trial with BNT111 and cemiplimab in combination or as single agents in patients with anti-PD-1/PD-L1-refractory/relapsed, unresectable Stage III or IV melanoma

Sponsor BioNTech SE

Start (EU)
Latest update
Estimated end
Operational learnings available1 trial-level finding · Read insights
  • A local CRO reporting error in Italy communicated an implausible BNT111 stability out-of-specification result as an urgent safety measure, resulting in a temporary clinical halt and enrollment suspension from 05 November to 17 December 2021.

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

Two part (double-blind inclisiran versus placebo [Year 1] followed by open-label inclisiran [Year 2]) randomized multicenter study to evaluate safety, tolerability and efficacy of inclisiran in children (2 to less than 12 years) with homozygous familial hypercholesterolemia and elevated LDL-cholesterol (ORION-19)

Sponsor Novartis Pharma AG

Start (EU)
Latest update
Estimated end

Two part (double-blind inclisiran versus placebo [Year 1] followed by open-label inclisiran [Year 2]]) randomized multicenter study to evaluate safety, tolerability and efficacy of inclisiran in children (6 to less than 12 years) with heterozygous familial hypercholesterolemia and elevated LDL-cholesterol (ORION-20)

Sponsor Novartis Pharma AG

Start (EU)
Latest update
Estimated end

Questions about this trial experience

What services are recorded for Abf Pharmaceutical Services?

The 2026-10-09 snapshot links Abf Pharmaceutical Services to 32 distinct CTIS trials. Recorded services include Medicinal product management, Laboratory services, Local depot for storage and distribution of AxMP to sites/ final Rec. + Destructionof used/unused IMP and AxMP, at EoT, This local vendor is used as local depot for storage and distribution of AxMP to sites and also for the final reconciliation and destruction of both, used and unused IMP and AxMP, at the end of the trial., among 24 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 Abf Pharmaceutical Services?

The most frequently recorded therapeutic areas are Solid Tumor Oncology, Cardiology, Immunology, Dermatology. Recorded phases include Phase 2, Phase 3, 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 Abf Pharmaceutical Services conducted?

The linked trials record locations in 25 countries, including Germany, Spain, Austria, France, Poland. These are trial locations, not confirmed office locations or countries where Abf Pharmaceutical Services delivered services.

What can this page tell me about Abf Pharmaceutical Services's trial experience?

Browse 32 distinct trials with recorded roles, sponsor names, available study dates and links to CTIS source records. 2 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 2 recorded name variants under Abf Pharmaceutical Services. Legacy brands remain separate unless explicitly matched in the name registry.

View recorded company names
  • ABF Pharmaceutical Services GmbH
  • Abf Pharmaceutical Services GmbH

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