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Printable Handouts
Navigable Slide Index
- Introduction
- Conflict of interest disclosure
- Table of contents
- Different types of PDMP
- Home-based SCIg treatment vs. hospital and home-based IVIg treatment
- Origin of plasma collected for fractionation
- Drivers for increasing demand
- Defined consequences and undefined solutions
- Evolution of hemophilia treatment
- Extended half-life products
- Gene therapy in hemophilia
- First market approved drug to treat hemophilia B
- FcRn inhibitors
- International comparisons
- International comparisons: demands in 2014
- Clinical value of PDMPs: observed benefits
- Clinical value of PDMPs: a growing number of clinical indications
- Increasing PDMPs consumption
- The global distribution of plasma collection
- The worldwide plasma proteins market by product
- Product mix in selected countries and regions 2020
- Product mix over five decades (1977–2027)
- Self-sufficiency in plasma-derived therapies: the Italian case (2020)
- The Italian Blood System and PDMPs
- Ig demand (g) per 1,000 inhabitants (Italy, 2020)
- Italian regional variation
- Albumin: total and regional demand 2017–2021
- Immunoglobulins: total and regional demand 2017–2021
- Antithrombin: total and regional demand 2017–2021
- Factor VIII: total and regional demand 2017–2021
- Prothrombin complex concentrates: total demand 2017–2021
- Fibrinogen: total and regional demand 2017–2021
- Immunoglobulin treatments
- Notable historic uses of antibody therapy against infectious diseases
- Evolution of passive immunotherapies against a novel pandemic microbe
- Convalescent plasma procurement
- Convalescent plasma management
- Content of convalescent plasma
- CCP in immunocompetent patients: summary of RCTs
- High titer CCP used early “works”
- CCP showed comparable efficacy at reducing hospitalizations in outpatients
- CCP was safe in a series of 105,000 US patients: <1% transfusion reactions
- CCP in immunocompromised patients: risk ratio
- CCP in immunocompromised patients
- Antibody therapy for COVID-19 after two years: take-home messages
- CCP “rescues” B-cell depleted patients with mAb treatment-emergent resistance
- VaxPlasma: high post-infusion Ab levels
- “VaxPlasma” RCT & heme malignancies
- BA.1 breakthrough (hybrid) VaxPlasma neutralizes BA.2 and BA.4/5
- Omicron is diversifying into a variant soup but converging
- Omicron mutations resistant to mAbs
- Anti-spike mAbs are ineffective
- Genomic surveillance and mAb resistance
- Current indications for CCP
- Hierarchy of evidence: convalescent plasma & COVID-19
- Thank you for your attention
Topics Covered
- Albumin
- Immunoglobulins (Ig)
- Clotting factors
- Hemophilia
- Plasma and plasma proteins
- COVID-19
- Convalescent plasma
- VaxPlasma
- Intravenous immunoglobulins (IVIG)
- Plasma collection
- The Italian Blood System
Links
Series:
Categories:
Therapeutic Areas:
External Links
Talk Citation
Focosi, D. (2023, June 29). The future of plasma-derived medicinal products (PDMP) [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved December 21, 2024, from https://doi.org/10.69645/EGVN9701.Export Citation (RIS)
Publication History
Financial Disclosures
- Dr. Daniele Focosi has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.
Other Talks in the Series: Periodic Reports: Advances in Clinical Interventions and Research Platforms
Transcript
Please wait while the transcript is being prepared...
0:00
Good morning, you all.
I'm Daniele Focosi.
I'm a hematologist and
transfusion physician at
the Pisa University
Hospital in Italy.
I'm going to talk to
you about the future of
plasma-derived medicinal
products or PDMP,
as we will shorten in
the rest of this talk.
0:21
I have no conflict
of interests to
disclose concerning the
topic of this talk.
0:29
I'm going to introduce
you to the table of
contents during
this one hour talk.
At first, we will
discuss the types of
PDMP and their main indications.
Then I will focus on the
Italian case study for
what concerns PDMP
usage and collections.
Then I will focus on
a special type of
PDMP which is COVID-19
convalescent plasma,
which is a topic of
utmost interests in
the last three years.
Finally, I will discuss
the perspectives for
the intravenous
immunoglobulins or
IVIG in the setting of COVID-19,
especially for the
immune-compromised patients.
1:20
At first, let's have a look at
the different types of PDMP.
The most used type is
definitively albumin,
which represents the main
protein in human serum.
Albumin has a half-life
as short as 12-16 hours,
and these are
commercially available
at two different concentrations.
The first one is
the isooncotic
formulation at 5%,
and the second formulation is
at 20-25% concentration,
so it is hyper-oncotic.
The main indications for
usage of albumins are
evacuative paracentesis,
high-volume therapeutic
plasmapheresis,
bacterial peritonitis, and as
a minor indications
albumin can also
be used in patients
with severe burns,
hemorrhagic shock,
major surgery,
protein-losing enteropathies,
and nephrotic syndrome.
The second most commonly use
PDMP, is immunoglobulins.
It is mostly used as an
intravenous formulation,
but it is increasingly used
as a subcutaneous formulation,
as we will see later.
There are three main
concentrations of immunoglobulins,
5, 10, and 50 g/l.
In commercially available
immunoglobulins
mostly consist of IgG
subclasses of immunoglobulin,
meaning that they are poorly
representative of IgA,
and IgM subclasses.
The main indications for
immunoglobulins are
primary and secondary
hypogammaglobulinemias as a
replacement therapy and at
high doses, the other
major indication
is instead autoimmune diseases.
The most common
autoimmune diseases are
ITP, Immune
Thrombocytopenic Purpura,
Guillain-Barre syndrome,
chronic inflammatory
demyelinating polyneuropathies
and Kawasaki syndrome.
These are the
official indications.
But most of the usage actually
stems from plenty
of off-label uses,
which is generating
scarcity of the product.
We are having in these
years a pipeline of
small molecules that will
hopefully reduce the demand
for immunoglobulins.
The main class is
the blockers of the
neonatal Fc receptor,
which basically
reduce the clearance
of the immunoglobulins
that are reinfused.
Then we have the third
major class of PDMP,
which are the clotting factors.
They are mainly used as
a replacement therapy in
patients with coagulopathies.
We have different types
of clotting factors.
The main two are Factor VIII
and Factor IX concentrates,
which are used for
hemophilia A and
hemophilia B respectively.
Factor VIII concentrates can
also include Von
Willebrand factor,
which is another very
important protein
for the stability
of coagulation.
Another side indication is
Von Willebrand disorder,
which is a different type
of inherited coagulant.
As you can see,
there are plenty of
different plasma derived
clotting factors
already available in the market.
But they are suffering
mounting competition from
recombinant clotting factors.
This basically means
that we can forecast a
reduction in the demand
for plasma-derived
clotting factors
from both recombinant
clotting factors
and upcoming gene therapies
for what concerns hemophilia.
But plasma-derived clotting
factors is not limited to
Factor VIII and IX
because we also
have prothrombin
complex concentrates,
which are also available
for different indications,
and we've quite a varied
formulation on the market.
Then we have other minor plasma
derived clotting factors,
such as antithrombin III,
and activated protein
C concentrates.
These do not represent
the majority of usage,
but can be somewhat
lifesaving so there
are often drugs
which can be very useful
in daily practice.