Presentation generale mars Syncrosome_JP
As more than 60% of new drugs fail in phase 2, we have chosen to focus
our activities since 2000 on preclinical In Vivo Efficacy Studies to offer
better predictability and anticipate clinical results. We are actively involved in
optimizing efficacy study designs on animal models to improve the
success rate in phase 2 and thus reduce the drug-to-market cost.
With advanced techniques selecting specific biomarkers and func-
tional exploration methods relying on strict procedures, trained
people and appropriate animal models, our team of outstanding pro-
fessionals look forward to assist our customers in evaluating the po-
tential of their compounds.
RICHARD MITRY
Founder & CEO
SYNCROSOME
2
Partner of large and medium drug discovery companies all around the
world since 2000, our main activities consist in :
DRUG EFFICACY STUDIES
BIOAVAILIBILITY AND CNS-PK
STUDIES
We have developped and validated so far more than 15 disease models,
and our flexible and human-sized organization can design and operate tai-
lored experimental protocols to give you appropriate answers.
Beyond sound science, our proactive approach combining
pharmacological expertise, appropriate study design, relevant
endpoints performed on relevant and complemental disease models,
provide our clients the most relevant datas.
Besides our premium services and track record of success, we pay
especial attention to ethics, animal welfare, sustainable development
and to the validation of up to date technics.
IN SHORT
3
OUR PRECLINICAL SERVICES
D I S E A
S E M
O D E L S
0 10 20
30
0
12
8
4
Cardiovascular monitoring, Inflammation,
Neuroprotection, Respiratory monitoring,
Behaviour tests, Gastrointestinal activity
4
Echocardiography, Plethysmography,
Laser doppler, Fluorescence
microscopy, Image analysis
ELISA, Histology, Enzyme activity, Cell
counting, Bioanalytical services,
Neuromediator monitoring
Special administration, Surgery suites,
Microdialysis, PK and Bioavailability,
Accredited vivarium, In vivo BBB
passage
PHYSIOLOGICAL BIOMARKERS FUNCTIONAL EXPLORATION
IN VIVO EXPERIMENTS
CELLULAR AND MOLECULAR
BIOMARKERS
DISEASE MODELS
Central nervous system :
Parkinson, Stroke, (CNS PK page 9)
Gastroenterology :
IBD, IBS, Ulcer, Emesis and/or Nausea, Intestinal
transit, Gastric emptying
Cardiovascular :
Arterial hypertension, Acute myocardial ischemia, Heart
failure, Blood loss
Metabolic Disorder :
Type 1 Diabetes, Type 2 Diabetes
Respiratory :
Asthma, Bronchitis, Cough, Pulmonary Arterial
Hypertension
DRUG EFFICACY STUDIES
5
PHARMACOKINETICS AND CNS-PK
CNS- PK
BBB passage
Brain to plasma ratio
Neurotransmitter concentration
Brain microdialysis
PK supporting efficacy assessment
Bioavailibilty from rodent to NHP
Bioanalysis
Various administration routes and organe or fluid sampling
6
KEY FACTS
Founded in 2000, owner of its facilities (lab, housing and offices)
Based in Marseille (3 hours away by train from Paris)
Near international airport Marseille Provence and Toulon airport with
transportation.
More than 350 studies carried so far, 180 customers.
Accredited facilities (N°B-1305529), laboratory and technical staff.
Member of the French Ethical Committee C2EA – 71
CIR Agreement
7
15 disease models in Several therapeutic areas, validated in house.
Additionnal parameters and Biomarkers analysis, for High Content Data.
Bioavailibility and CNS-PK studies.
Development of tailored models with validation steps.
Proactive approach in study design, experimental stage and data interpretation with dedicated
study directors for each Dpt.
GLP-like laboratory
KEEP IN MIND…
8
TESTIMONIALS
We were looking for a few months for a company able to help us
in making the right decision with our in house compounds.
Our discussions with Syncrosome were very fruitfull and were
always available to give us their feedback and suggestions. They are
focus on in vivo efficacy studies for more than 10 years with a
comprehensive background. In summary « good procedures for good
science»
allowed us to succed in phase 2. Very good guys, thank you !
M.T., Target Validation, CHIESI Farmaceutici S.p.a.
We wanted to collaborate with a high level CRO capable of
conducting in vivo studies in a good scientific manner, and to assist us in
elaborating the study design and interpretation of results. We retained
Syncrosome after visting their facilities that they fully own. We also
audit their pro- cedures, SOP, training program etc… Everything was
OK. We had very good relationship with the Study director and good
discussions before, during and after the experiments !
C.P. Director Research and Preclinical, HELSINN
10
SOME OF OUR REFERENCES
Angelini
Astra Zeneca
Athera
Boiron
Boehringer Ingelheim
Celladon
Chiesi
Esteve
Euroscreen
GSK
Helsinn
Innate Pharma
Janssen
Materia Medica Holding
Nicox
Novartis
Nycomed
Original Process
Polyphor
Rempex Pharmaceuticals
Roche
Sanofi
1
1
Presentation generale mars Syncrosome_JP

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Presentation generale mars Syncrosome_JP

  • 2. As more than 60% of new drugs fail in phase 2, we have chosen to focus our activities since 2000 on preclinical In Vivo Efficacy Studies to offer better predictability and anticipate clinical results. We are actively involved in optimizing efficacy study designs on animal models to improve the success rate in phase 2 and thus reduce the drug-to-market cost. With advanced techniques selecting specific biomarkers and func- tional exploration methods relying on strict procedures, trained people and appropriate animal models, our team of outstanding pro- fessionals look forward to assist our customers in evaluating the po- tential of their compounds. RICHARD MITRY Founder & CEO SYNCROSOME 2
  • 3. Partner of large and medium drug discovery companies all around the world since 2000, our main activities consist in : DRUG EFFICACY STUDIES BIOAVAILIBILITY AND CNS-PK STUDIES We have developped and validated so far more than 15 disease models, and our flexible and human-sized organization can design and operate tai- lored experimental protocols to give you appropriate answers. Beyond sound science, our proactive approach combining pharmacological expertise, appropriate study design, relevant endpoints performed on relevant and complemental disease models, provide our clients the most relevant datas. Besides our premium services and track record of success, we pay especial attention to ethics, animal welfare, sustainable development and to the validation of up to date technics. IN SHORT 3
  • 4. OUR PRECLINICAL SERVICES D I S E A S E M O D E L S 0 10 20 30 0 12 8 4 Cardiovascular monitoring, Inflammation, Neuroprotection, Respiratory monitoring, Behaviour tests, Gastrointestinal activity 4 Echocardiography, Plethysmography, Laser doppler, Fluorescence microscopy, Image analysis ELISA, Histology, Enzyme activity, Cell counting, Bioanalytical services, Neuromediator monitoring Special administration, Surgery suites, Microdialysis, PK and Bioavailability, Accredited vivarium, In vivo BBB passage PHYSIOLOGICAL BIOMARKERS FUNCTIONAL EXPLORATION IN VIVO EXPERIMENTS CELLULAR AND MOLECULAR BIOMARKERS DISEASE MODELS
  • 5. Central nervous system : Parkinson, Stroke, (CNS PK page 9) Gastroenterology : IBD, IBS, Ulcer, Emesis and/or Nausea, Intestinal transit, Gastric emptying Cardiovascular : Arterial hypertension, Acute myocardial ischemia, Heart failure, Blood loss Metabolic Disorder : Type 1 Diabetes, Type 2 Diabetes Respiratory : Asthma, Bronchitis, Cough, Pulmonary Arterial Hypertension DRUG EFFICACY STUDIES 5
  • 6. PHARMACOKINETICS AND CNS-PK CNS- PK BBB passage Brain to plasma ratio Neurotransmitter concentration Brain microdialysis PK supporting efficacy assessment Bioavailibilty from rodent to NHP Bioanalysis Various administration routes and organe or fluid sampling 6
  • 7. KEY FACTS Founded in 2000, owner of its facilities (lab, housing and offices) Based in Marseille (3 hours away by train from Paris) Near international airport Marseille Provence and Toulon airport with transportation. More than 350 studies carried so far, 180 customers. Accredited facilities (N°B-1305529), laboratory and technical staff. Member of the French Ethical Committee C2EA – 71 CIR Agreement 7
  • 8. 15 disease models in Several therapeutic areas, validated in house. Additionnal parameters and Biomarkers analysis, for High Content Data. Bioavailibility and CNS-PK studies. Development of tailored models with validation steps. Proactive approach in study design, experimental stage and data interpretation with dedicated study directors for each Dpt. GLP-like laboratory KEEP IN MIND… 8
  • 9. TESTIMONIALS We were looking for a few months for a company able to help us in making the right decision with our in house compounds. Our discussions with Syncrosome were very fruitfull and were always available to give us their feedback and suggestions. They are focus on in vivo efficacy studies for more than 10 years with a comprehensive background. In summary « good procedures for good science» allowed us to succed in phase 2. Very good guys, thank you ! M.T., Target Validation, CHIESI Farmaceutici S.p.a. We wanted to collaborate with a high level CRO capable of conducting in vivo studies in a good scientific manner, and to assist us in elaborating the study design and interpretation of results. We retained Syncrosome after visting their facilities that they fully own. We also audit their pro- cedures, SOP, training program etc… Everything was OK. We had very good relationship with the Study director and good discussions before, during and after the experiments ! C.P. Director Research and Preclinical, HELSINN 10
  • 10. SOME OF OUR REFERENCES Angelini Astra Zeneca Athera Boiron Boehringer Ingelheim Celladon Chiesi Esteve Euroscreen GSK Helsinn Innate Pharma Janssen Materia Medica Holding Nicox Novartis Nycomed Original Process Polyphor Rempex Pharmaceuticals Roche Sanofi 1 1