Evidence map›Paper›PMID 31621991›Full record

Trial reportHaemophilia : the official journal of the World Federation of Hemophilia2019

BAY 94-9027 prophylaxis is efficacious and well tolerated for up to >5 years with extended dosing intervals: PROTECT VIII extension interim results.

Shadan Lalezari, Mark T Reding, Ingrid Pabinger, Pal Andre Holme, Claude Negrier, Pavani Chalasani, Ho-Jin Shin, Maria Wang, Despina Tseneklidou-Stoeter, Monika Maas Enriquez

Registry-linked trialAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in Haemophilia : the official journal of the World Federation of Hemophilia, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01580293 (A Phase II/III, Multicenter, Partially Randomized, Open Label Trial Investigating Safety and Efficacy of On-demand and Prophylactic Treatment With BAY94-9027 in Severe Hemophilia A), which is not on this map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT01580293 phase2 / phase3completednot on this map

A Phase II/III, Multicenter, Partially Randomized, Open Label Trial Investigating Safety and Efficacy of On-demand and Prophylactic Treatment With BAY94-9027 in Severe Hemophilia A

TypeinterventionalSponsorBayerRan2012 to 2019Enrolled145ConditionsHemophilia AArmsBAY94-9027
3 · Its place in the literature

Who cites it

14 citing papers in PubMed.

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  13. Target joint resolution in patients with haemophilia A receiving long-term prophylaxis with BAY 94-9027.Haemophilia : the official journal of the World Federation of Hemophilia · 2020
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  14. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Shadan LalezariIsrael National Hemophilia Center, Chaim Sheba Medical Center, Sackler School of Medicine, Tel-Aviv University, Tel Hashomer, Israel.ORCID https://orcid.org/0000-0002-6112-1127
Mark T RedingCenter for Bleeding and Clotting Disorders, University of Minnesota Medical Center, Minneapolis, MN, USA.
Ingrid PabingerClinical Division of Haematology and Haemostaseology, Department of Medicine I, Medical University of Vienna, Vienna, Austria.
Pal Andre HolmeDepartment of Haematology, Oslo University Hospital, Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
Claude NegrierHemophilia Comprehensive Care Center and Hematology Department, Louis Pradel University Hospital, Lyon, France.ORCID https://orcid.org/0000-0002-2905-055X
Pavani ChalasaniUniversity of Arizona Cancer Center, Tucson, AZ, USA.
Ho-Jin ShinDivision of Hematology-Oncology, Department of Internal Medicine, Pusan National University School of Medicine, Pusan National University Hospital, Busan, Korea.
Maria WangBayer, Whippany, NJ, USA.
Despina Tseneklidou-StoeterBayer, Berlin, Germany.
Monika Maas EnriquezBayer, Wuppertal, Germany.

Funding

BayerDarwin
6 · The paper itself

Abstract

introductionBAY 94-9027 is an extended-half-life, site-specifically PEGylated, B-domain-deleted recombinant factor VIII (FVIII). The PROTECT VIII main study demonstrated efficacy of bleed control using extended-interval prophylaxis with BAY 94-9027 for 36 weeks.

aimTo report long-term efficacy and safety of prophylaxis with BAY 94-9027 in a descriptive analysis of the ongoing PROTECT VIII extension with a total treatment time of up to >5 years.

methodsPreviously treated males aged 12-65 years with severe haemophilia A who completed the PROTECT VIII main study were eligible for the open-label extension. Patients received on-demand treatment or prophylaxis (30-40 IU/kg twice weekly, 45-60 IU/kg every 5 days, or 60 IU/kg every 7 days) and could switch regimens as needed.

resultsPatients (N = 121; on demand, n = 14; prophylaxis, n = 107) accumulated a median (range) of 3.9 years (297-1965 days) and 223 (23-563) total exposure days by 31 January 2018. During the extension, median (quartile [Q]1; Q3) annualized bleeding rates (ABRs) for total bleeds were 1.6 (0.3; 4.6) for patients receiving prophylaxis and 34.1 (20.3; 36.6) for patients receiving on-demand treatment. ABRs for twice-weekly (n = 23), every-5-days (n = 33), every-7-days (n = 23) and variable frequency (n = 28) treatments were 1.7, 1.2, 0.7 and 3.1, respectively. Of prophylaxis patients, 20.6% were bleed-free throughout the extension (median time, 3.2 years), and 44.5% were bleed-free during the last 6 months. No patients developed FVIII inhibitors.

conclusionsBAY 94-9027 prophylaxis was efficacious and well tolerated with dosing intervals up to every 7 days for a median (range) of 3.9 years (0.8-5.4 years).

Indexed as

SafetyAdolescentAdultChildDose-Response Relationship, DrugFactor VIIIFemaleHemophilia AHemorrhageHumansMaleMiddle AgedPolyethylene GlycolsTime FactorsYoung AdultBAY 94-9027Factor VIIIPolyethylene Glycolsclinical trialfactor VIIIhaemophilia Aintravenous infusionsrecombinant proteins

Identifiers

PMID31621991
PMCPMC6900134

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.