RICHARD L. MITCHELL, PH.D.
15920 177th Avenue
N.E.
Home: (425) 402-6341
Woodinville, WA 98072
Cell: (425) 922-1393
Email: richard.mitchell@verizon.net
SCIENTIFIC
DIRECTOR, MARKETING AND
BUSINESS DEVELOPMENT
PROFILE
Articulate professional with 22
years of broad scientific and
business development
leadership. Demonstrated
success in forging partnerships
with pharmaceutical and
biotechnology companies and
establishing academic
collaborations to solve unmet
technical and medical needs.
Experienced educator and public
speaker acting as a liaison
between laboratory, business,
and academic leaders.
STRATEGIC PLANNING &
IMPLEMENTATION
·
Business strategy and
development
·
Technology licensing and company
acquisitions
·
Marketing, competitive
intelligence
·
Outstanding presentation skills
·
Establish collaborations,
partnerships, consultancies
·
Technical, medical, scientific,
and academic liaison with
college teaching experience
·
Due diligence of delivery
technology, therapeutics, and
intellectual property
acquisitions
·
Expertise in microbiology,
molecular virology and oncology,
molecular pharmacology, drug
delivery, and drug
discovery/development
technologies applied to small
molecule and peptide
therapeutics
·
siRNA target selection and
siRNA delivery for viral
infections, cancer, inflammation
and immunomodulation targets
Nastech Pharmaceutical Company
Inc.
- Bothell,
WA
April 2006 - Present
SCIENTIFIC DIRECTOR, MARKETING
AND BUSINESS DEVELOPMENT
(reporting to Chief Business
Officer)
·
Provided strategic leadership to
broaden core drug delivery
capabilities, initiated
acquisition efforts with several
companies, progressing several
to negotiated offers (~$25MM -
$100MM)
·
Identified potential partners
for proprietary therapeutics and
managed relationships, drafting
and providing preclinical and
clinical data packages for
prospective partners
·
Initiated drug delivery
feasibility collaborations
leading to partnerships
including one entering the
clinic in 2008
·
Completed drug delivery
technology evaluations for over
100 companies and technologies
covering multiple delivery
routes including buccal, oral,
pulmonary, nasal, transdermal,
and parenteral/sustained-release
injectables
o
Recommended four of these for
significant partnership or
acquisition activity
·
Technology acquisition efforts
led to signed technology
partnerships (e.g. formulation
technology applied to sustained
drug release and vaccine
delivery)
·
Presented Nastech drug delivery
technology and therapeutic drug
programs to medical, scientific,
and business audiences
o
Diabetes, obesity, osteoporosis,
autism; siRNA therapeutic
targets
o
Non-invasive peptide/protein
drug delivery technologies,
siRNA delivery
Shoreline
Community College
- Shoreline,
WA
January – March 2006
ASSOCIATE FACULTY MEMBER
(Temporary)
·
Prepared curriculum and taught
full-time recombinant DNA course
(lecture and laboratory)
Adnavance
Technologies, Paracelsus
Technologies
– Vancouver, BC,
Canada March 2006
CONSULTANT
(Temporary)
(Reporting to CEO AND CFO)
·
Consulted with academic and
industry thought leaders
·
Recommended corporate
development strategy based on
in-depth assessment of bacterial
and viral infectious disease
targets for proprietary
electrochemical DNA sensor
technology (Adnavance) and
DNA-vaccine technology
(Paracelsus)
·
Offered position of VP of
Business Development by CEO and
CFO following assignment
MDS Pharma Services
(formerly Panlabs, Inc.) -
Bothell,
WA
1990 - 2005
SENIOR DIRECTOR, STRATEGIC
ALLIANCES
SENIOR DIRECTOR OF PHARMACOLOGY
DIRECTOR OF PHARMACOLOGY,
PHARMACOLOGY PRODUCT TEAM LEADER
PRINCIPAL SCIENTIST,
PHARMACOLOGY PRODUCT TEAM LEADER
SENIOR SCIENTIST
·
Supervised laboratory staff,
planned and organized lab
activities and set performance
metrics
·
Grew revenues >15-fold ($1.5 MM
- $25 MM/yr) as Pharmacology
Product Team Leader
·
Identified acquisition
opportunities and provided
technology due diligence for MDS
Capital, MDS Pharma Services,
and MDS Sciex
·
Identified and initiated
acquisition efforts
o
Skeletech Inc. (preclinical CRO)
~$10 MM acquisition (2005)
o
Signature Biosciences (cellular
dielectric spectroscopy)
acquired by MDS Sciex
·
Identified, negotiated, guided
collaborations
o
Iconix Pharmaceuticals-MDS PS
Chemoinformatics Database
Collaboration (Collaboration
Board Member)
o
BioSource – MDS PS Strategic
Alliance; initiated, drafted &
negotiated
o
Becton Dickenson (BD)-MDS Pharma
Services Biomarker Alliance
·
Secured, managed pharma and
biotech client relationships
(e.g. managed/advised/technical
liaison to Merck on preclinical
testing strategies)
·
Led assay development team
developing >400 pharmacology
tests
·
Trained sales staff (approx. 3
face-to-face training sessions
per year)
·
Delivered sales presentations
(Asia, Europe, US) and provided
technical sales support
·
Performed technology due
diligence for MDS Capital Corp.
(Amnis, Ambit, Aurora BioMed,
Signature BioSciences, Specialty
Laboratories, Nodality and
others)
·
Conceived, designed & built key
innovative IT systems & sales
tools including:
o
Fully integrated client data
delivery system and web
interface
o
MDS Panlabs corporate website
o
MDS Panlabs sales team website
o
Automated sales quoting and
tracking system (automated
quoting and tracked performance
vs. sales metrics and
objectives)
o
Designed and developed automated
sales aids (facilitated
technical sales process)
·
NIH Phase I SBIR Grant:#1 R43 DA
09203-01 (Signal Transduction by
Peripheral Cannabinoid
Receptors) – wrote pharmacology
section of Phase I SBIR grant,
performed pharmacology work
(1994)
California Biotechnology Inc.
(Scios Inc., Johnson & Johnson)
– Mt. View, CA
1988 - 1990
SENIOR SCIENTIST
SCIENTIST
·
Cloned and expressed genes
encoding angiogenic growth
factors (aFGF, bFGF, VEGF)
·
Supervised laboratory staff
·
Wrote sections of patents, IND
filings; scientific
presentations
Washington State Business
License:
#
602544570 for Touching Light
Photography, a sole
proprietorship established in
2005. (www.touchinglightphotography.com)
· NIH
Postdoctoral Fellowship,
The Salk Institute For
Biological Studies, La Jolla, CA
1984 - 1986
·
Ph.D., Microbiology
(virology/molecular biology
focus) Univ. of Minnesota,
Minneapolis, MN 1984
·
Ph.D. Program, Microbiology
(immunology/virology focus)
Univ. of Iowa, Iowa City, IA
1976-1978
·
B.A., Biology
(Honors in the Major, College
Honors) University of
California, Santa Cruz, CA 1976
·
Additional course: From
Laboratory to Leadership,
Washington Biotechnology and
Biomedical Association (WBBA)
(1999).
·
Additional course: Principles
of Toxicokinetics and
Pharmacokinetics.
University of Arizona. 2007.
Co-Inventor on Submitted
Patent: Mitchell, R., Mulligan,
J., Castillo, G. 2005.
International Application
WO2005069725
"Fluorescence-Based ADP
Detection System"
Co-Inventor on US Patent:
Tischer, E.G., J.A. Abraham,
J.C. Fiddes, R.L. Mitchell.
1993. U.S. Patent No. 5,219,739
for "DNA sequences encoding
BVEGF120 and HVEGF121 and
methods for the production of
bovine and human vascular
endothelial cell growth factors,
BVEGF120 and HVEGF121".
Co-Inventor on US Patent:
Tischer, E.G., J.A. Abraham,
J.C. Fiddes, R.L. Mitchell.
1992. U.S. Patent No. 5,194,596
for "Production of vascular
endothelial cell growth
factor".
FELLOWSHIPS, AWARDS,
DISTINCTIONS
·
Customer Satisfaction Award, MDS
Pharma Services (2002)
·
CalBio Professional Recognition
Award for Outstanding
Achievement (1989)
·
Bacaner Research Award (for
outstanding thesis) Minn. Med.
Foundation, Univ. of Minn.
(1985)
·
NIH Individual Postdoctoral
Fellowship Award, The Salk
Institute, San Diego
(1984–1987)
·
USPHS Predoctoral Fellowship,
Dept. of Microbiology, Univ. of
Minn. (1978-1982)
·
Honors in Biology and College
Honors, University of
California, Santa Cruz (1976)
Mitchell, R.L., Lai, Y., Mackie,
K.P., and Thomsen, W.J. Phase I
Small Business Innovative
Research Grant (NIH) #1 R43 DA
09203-01 Signal Transduction by
Peripheral Cannabinoid
Receptors, 1994.
PROFESSIONAL AFFILIATIONS
·
The Endocrine Society
·
Society for Neuroscience
·
The Obesity Society
·
American Society for
Pharmacology and Experimental
Therapeutics
·
American Association of
Pharmaceutical Scientists
·
Licensing Executives Society
·
Photographic Society of America
·
Member, Institutional Animal
Care and Use Committee (2006 –
present)
·
Chair, MDS PS Scientific
Advisory Committee 2004 – 2005
·
Chair, Shoreline Community
College Biotechnology Advisory
Committee 1997 - 2002
·
Member, Radiotherapeutic Build
Team, MDS Nordion, developing
Bexxar™ and Zevalin™
·
Member, Iconix-MDS Collaboration
Management Board (for
chemoinformatic database)
·
Chairman, Panlab's Safety
Committee, Vice-Chairman 1993 –
1994
Mitchell, R.L., Costantino,
H.R., Sileno, A., Duffy, T.,
Brandt, G., Quay, S.C. 2008.
Intranasal Insulin: PK Profile
Designed Specifically for
Prandial Treatment of Type 2
Diabetes. Drug Development
Research 69(3):143-152. (link)
Chiu, P.J.S., Marcoe, K.F.,
Bounds, S.E., Lin, C.-H., Feng,
J.-J., Lin, A., Cheng, F.-C.,
Crumb, W.J., Mitchell, R. 2004.
Validation of a [3H]Astemizole
Binding Assay in HEK293 Cells
Expressing HERG K+
Channels. J. Pharmacol. Sci..
95:311-319.
Herz, J.M., Thomsen, W.J.,
Mitchell, R., and Yarbrough, G.G.
1996. Receptors for Drugs.
Encyclopedia of Pharmaceutical
Technology, J. Swarbrick and
J.C. Boylan eds. vol. 13,
Marcel Dekker, Inc., New York.
Hill, P., Lai, Y., Hnilo, J.,
Lin, C-C., Karla, M., Bounds,
S., Middlemas, D., Herz, J.,
Mitchell, R.L. 1996. Cloning,
expression, and comparison of
the binding characteristics of
the known human dopamine
receptors. Advances in Neurology
69:41-52, Lippencott-Raven,
Philadelphia.
Felder, C.C., Joyce, K.E.,
Briley, E.M., Mansouri, J.,
Mackie, K., Lai, Y., Mitchell,
R.L., Ma, A.L. 1995. Comparison
of the pharmacology and signal
transduction of the human
cannabinoid CB1 and CB2
Receptors. Mol. Pharm.
48(3):443-450.
Mackie, K., Lai, Y., Westenbroek,
R., Mitchell, R.. 1995.
Cannabinoids activate an
inwardly rectifying potassium
conductance and inhibit non-L,N,P,T
type voltage-dependent calcium
currents in AtT20 cells
transfected with rat brain
cannabinoid receptor. J.
Neuroscience 15(10):6552-6561.
Tischer, E., Mitchell, R.,
Hartman, T., Silva, M.,
Gospodarowicz, D., Fiddes, J. C.
and Abraham, J. A., 1991. The
human gene for vascular
endothelial growth factor:
Multiple protein forms are
encoded through alternative exon
splicing. J. Biol. Chem.
266:11947-11954.
Tischer, E., Gospodarowicz, D.,
Mitchell, R. L., Silva, M.,
Schilling, J., Lau, K., Crisp,
T., Fiddes, J. C., and Abraham,
J. A.. 1989. Vascular
endothelial growth factor: A
new member of the
platelet-derived growth factor
gene family. Biochem. Biophys.
Res. Commun. 165:1198-1206.
Blam, S. B., Mitchell, R.,
Tischer, E., Rubin, J. S.,
Silva, Silver, M., S., Fiddes,
J. C., Abraham, J., Aaronson,
S.. 1988. Addition of growth
hormone secretion signal to
basic fibroblast growth factor
results in cell transformation
and secretion of aberrant forms
of the protein. Oncogene
3:129-136.
Neufeld, G., Mitchell, R.,
Ponte, P., and Gospodarowicz,
D.. 1988. Expression of human
basic fibroblast growth factor
cDNA in baby hamster
kidney-derived cells results in
autonomous cell growth. J.
Cell. Biol. 106:1385-1394.
Ferrara, N., Schweigerer, L.,
Neufeld, G., Mitchell, R., and
Gospodarowicz, D.
1987. Pituitary follicular
cells produce basic fibroblast
growth factor. Proc. Natl.
Acad. Sci.
USA 84:5773-5777.
Neufeld, G., Ferrara, N.,
Schweigerer, L., Mitchell, R.,
and Gospodarowicz, D.
1987. Bovine granulosa cells
produce basic fibroblast growth
factor. Endocrinology
121:597-603.
Mitchell, R. L., Hanks, S. K.,
and Verma, I. M. 1987. "Protooncogene
fos: An inducible multifaceted
gene". In: Symposium on
fundamental cancer research,
Vol. 39, pp99-113. University
of Texas System Cancer Center.
Billestrup, N., Mitchell, R. L.,
Vale, W., and Verma, I. M.
1987. "Growth hormone releasing
factor induces c-fos expression
in cultured primary pituitary
cells". Molecular Endocrinology
1: 300-305.
Van Beveren, C., Mitchell, R.
L., Henning-Chubb, C., Huberman,
E., and Verma, I. M. 1987.
"Expression of the c-fos gene
during differentiation". Adv.
Exp. Med. Biol. 213:263-274.
Mitchell R. L., Henning-Chubb,
C., Huberman, E., and Verma, I.
M. 1987. "c-fos expression is
neither sufficient nor
obligatory for differentiation
of monomyelocytes to
macrophages". Cell 45:497-504.
Verma, I. M., Mitchell, R. L.,
Sassone-Corsi, P. 1986.
Proto-oncogene fos: an
inducible gene. Princess
Takamatsu Symposium 17:279-290.
Mitchell, R. L., Kruijer, W.,
Schubert, D., Van Beveren, C.,
and Verma, I. M..
1986. "Structure and expression
of protooncogene fos". In:
Proceedings of the Seventh
International Symposium on Host
Defense Mechanisms Against
Cancer. Excerpta Medica, Tokyo.
Mitchell, R. L. 1986. "Post
development intensification of
autoradiographs". BRL Focus
8(3):10-11.
Coussens, L., Van Beveren, C.,
Smith, D., Chen, E., Mitchell,
R. L., Isacke, C. M., Verma, I.
M., and Ulrich, A. 1986.
"Molecular architecture of
receptor proto-oncogene fms:
Structural alteration of viral
homologue at carboxyl
terminus". Nature 320:
277-280.
Verma, I. M., Mitchell, R. L.,
Kruijer, W., Van Beveren, C.,
Zokas, L., Hunter, T., and
Cooper, J. A. 1985. "Protooncogene
fos: Induction and regulation
during growth and
differentiation. Cancer Cells.
3: Growth factors and
transformation". Feramisco, J.,
B. Ozanne, and C. Stiles, Eds.
Cold Spring Harbor Laboratory,
New York. pp 275-287.
Mitchell, R. L., Zokas, L.,
Schreiber, R. D., and Verma, I.
M.. 1985. "Rapid induction of
the expression of proto-oncogene
fos during human monocyte
differentiation". Cell 40:
209-217.
Deschamps, J., Mitchell, R. L.,
Meijlink, F., Kruijer, W.,
Schubert, D., and Verma, I. M.
1985. "Proto-oncogene fos is
expressed during development,
differentiation, and growth".
Cold Spring Harbor Symposia on
Quantitative Biology 50:
733-745.
Krzyzek, R. A., Mitchell, R. L.,
Lau, A. F., and Faras, A. J.
1980. "Association of pp60src
and src protein kinase activity
with the plasma membrane of
nonpermissive and permissive
avian sarcoma virus-infected
cells". J. Virol. 36: 805-815.
Crouch, N.A., and Mitchell, R.
L. 1978. "Replication of
vesicular stomatitis virus is
facilitated by Shope fibroma
virus in vivo". Infect. Imm.
25: 213-219.
Lautermilchn N., Bishopn A.,
Marcoen K., Boundsn S., Linn
C-H., Fengn J-J., Linn A.,
Chengn F-C., Mitchelln R., Chiun
P., Baumgartnern J. 2005.
Comparison of a hERG Binding
Assay with Automated Patch Clamp
Using the PatchXpress 7000A.
Soc. Biolmol. Screening Ann.
Mtg. P07036
Marcoe, K.F., Mitchell, R.L.,
Baumgartner, J.W. Binding
Affinity of Amyloidogenic,
Inflammatory and Antimicrobial
Immunogenic Peptide Ligands to
the Formyl Peptide Receptor-Like
1. 2004. Soc Biomol. Screening
Annual Mtg.
Shen, E., Mulligan, J.,
Castillo, G., Mitchell, R. 2004.
FastKinaseTM for Rapid
Determination of Multiple IC50
Profiles in a Panel of 24
Kinases. Soc. Biol. Screening
Ann. Mtg.
Bounds, S., Mitchell, R. 2004.
Development of High Throughput
Matrix Metalloproteinase
Activity Assays. Soc. Biolmol.
Screening Ann. Mtg.
P. Chiu, F-C.
Cheng, A. Lin, K-K.
Chang, R. Mitchell, N. Share, D.
Menard. 2004. An Integrated
Approach to Screen for
Anti-Diabetic Agents. Soc.
Biolmol. Screening Ann. Mtg.
Marcoe, K.F. and Mitchell, R.L.
2004. A High Throughput
Radioligand Binding Assay for
the Leptin OB-Rb Receptor. Soc.
Biolmol. Screening Ann. Mtg.
Marcoe, K.F., Mitchell, R.L.,
Baumgartner, J.W. 2004. Binding
affinity of amyloidogenic,
inflammatory and antimicrobial
immunogenic peptide ligands to
the formyl peptide receptor-like
1. Soc. Biomol. Screening 10th
Annual Conference
Martel, L., Mulligan, J.,
Castillo, G., Mitchell, R.,
Baumgartner, J. 2004.
Pharmacological characterization
of Eph receptor tyrosine kinases
with anti-angiogenic agent
genistein. Soc. Biomol.
Screening 10th Annual
Conference.
Mulligan, J. Castillo, G.,
Mitchell. R.L. 2003.
Characterization of Cathepsin
Substrate and Inhibitor
Specificities. Soc. Biol.
Screening Ann. Mtg.
Gee, P., Mitchell, R., Browne,
L., Kolaja, K., Jarnagin, K.,
Natsoulis, G., Roter, A. 2003.
DrugMatrix™ provides predictive
chemogenomics solutions for
safety assessment in drug
discovery and development.
Eurotox 2003, Florence, Italy.
Abstract 213.
Y. Lai, Mackie, K., Mitchell,
R. 1994. Cannabinoids activate
an inwardly rectifying potassium
conductance and inhibit a
calcium current in AtT20 cells
expressing rat cannabinoid
receptor. Can. J. Physiol.
Pharmacol. 72 (Suppl. 1):423.
P. Hill, ,Y., Hnilo, J.,
Middlemas, D. S., Lin, C., Hsing,
H., Leung, F., Karla, M.,
Bounds, S., Herz, J., Chen, C.,
Mitchell, R. 1994. Comparison
of binding characteristics of
the known human dopamine
receptors. Can. J. Physiol.
Pharmacol. 72 (Suppl. 1):383.
Mitchell, R.L., Hill, P., Lai,
Y., Hnilo, J., Lin, C., Hsing,
H., Leung, F., Karla, M.,
Bounds, S., Middlemas, D., Herz,
J. 1994. Cloning, expression,
and comparison of the binding
characteristics of the known
human dopamine receptors. 11th
International Symposium on
Parkinson's Disease, Rome.
Mitchell, R. 1994. Human U937
promonocytes express an
alternatively spliced mRNA
encoding a shortened isoform of
cytosolic phospholipase A2.
FASEB J. 8(4):A217.
Middlemas, D. S., Hill, P., Lai,
Y., Hnilo, J., Lin, C., Hsing,
H., Leung, F., Karla, M.,
Bounds, S., Herz, J., Chen, C.,
and Mitchell, R. 1994.
Comparison of binding
characteristics of the known
human dopamine receptors. FASEB
J. 8(4):A106.
Lai, Y., Mackie, K., Mitchell,
R. 1994. Cannabinoids activate
an inwardly rectifying potassium
conductance in AtT20 cells
expressing rat cannabinoid
receptor. FASEB J. 8(4):A381.
Hill, P. A., and Mitchell, R.
L. 1994. Characterization of
phosphodiesterase activity from
U937 cells. FASEB J. 8(4):A217.
Bounds, S., Hill, P., and
Mitchell, R. 1994. Development
of a glucocorticoid receptor
transcription response element (GTRE)
assay. FASEB J. 8(5):A650.
Hnilo, J. M., Mitchell, R. L.,
Hill, P. A., Crawford, M. S.
1991. Development of functional
tyrosine kinase assays based on
EGF and PDGF receptor
cytoplasmic domains expressed in
Sf9 insect cells. The
Pharmacologist 33:174.
Mitchell, R. L., Hnilo, J. M.,
Maechler, L., Crawford, M. S.
1991. Development of functional
tyrosine kinase assays based on
EGF and PDGF receptor
cytoplasmic domains expressed in
Sf9 insect cells. Sixth S.E.
Asia/W. Pacific Regional Mtg. of
Pharmacologists.
Hnilo, J. M., Mitchell, R. L.,
Maechler, L., Crawford, M. S.
1991. Development of a
functional tyrosine kinase assay
based on EGF receptor tyrosine
kinase domain expressed in Sf9
insect cells. Soc. Indus.
Microbiol. Ann. Mtg., 1991.
Mitchell, R. L., Silver, S.,
Abraham, J. A., Fiddes, J. C.
1988. CHO cells transfected
with basic fibroblast growth
factor linked to growth hormone
secretion signal efficiently
secrete 18 kD FGF and several
modified forms of the protein.
NCI-FCRF Fourth Ann. Mtg. On
Oncogenes p429.
Blam, S. B., Mitchell, R.,
Tischer, E., Rubin, J. S.,
Silva, M., Silver, S., Fiddes,
J. C., Abraham, J. A., Aaronson,
S. A. 1988. Addition of growth
hormone secretion signal to
basic fibroblast growth factor
results in cell transformation
and secretion of aberrant forms
of the protein. NCI-FCRF Fourth
Ann. Mtg. on Oncogenes p24.
Mitchell, R. L., Henning-Chubb,
C., Huberman, E., and Verma, I.
M. 1987. c-fos expression is
neither sufficient nor
obligatory for differentiation
of monomyelocytes to
macrophages. In: 1987 Year
Book of Cancer, Year Book
Medical Publishers, Houston.
Mitchell, R. L., Hanks, S. K.,
Henning-Chubb, C., Huberman, E.,
and Verma, I. M. 1986. Role of
the protooncogene fos during
growth and differentiation.
NCI-FCRF Second Ann. Mtg. On
Oncogenes.
Mitchell, R. L., and Verma, I.
M. 1985. Expression of the
protooncogenes c-fos and c-fms
during hematopoietic
differentiation. NCI-FCRF First
Annual Mtg. on Oncogenes.
Lau, A., Faras, A., Mitchell,
R., and Collins, C. 1981. ASV
transformed and revertant field
vole cells: pp60src, cellular
protein substrates, and
arrangement of the integrated
ASV genome. 1991 Ann. Mtg. on
RNA Tumor Viruses. Cold Spring
Harbor Laboratories.
Crouch, N. A., and Mitchell, R.
L. 1978. Facilitative effect of
Shope fibroma virus on the
replication of vescicular
stomatitis virus in vivo. Abs.
of the 78th Ann. Mtg. of the Am.
Soc. Microbiol.
SPEAKING ENGAGEMENTS
(RECENT/SCHEDULED):
TIDES 2008,
Las Vegas, NV. Update on
Intranasal Insulin Clinical
Trials: Ideal Pharmacokinetics
for Prandial Insulin in Type 2
Diabetics. (May 2008).
Natural Peptides to Drugs -
International Congress,
Zermatt, Switzerland. Invited
Plenary Lecture. (April 14-18,
2008).
American Society for
Pharmacology and Experimental
Therapeutics 2008.
(ASPET): Role of Oxytocin in
Autistic Spectrum Disorder, and
the Development of Intranasal
Carbetocin as a Potential
Therapeutic for Autism and
Asperger's. Invited speaker.
(March 2008).
Drug Delivery Partnerships.
San Diego, CA. How to Pursue
and Assess Potential
Technologies as Synergistic Fits
for Your Program. Invited
panelist. (January 21, 2008).
Invited Speaker, 3rd Annual
Metabolic Diseases World Summit,
San Diego, CA Intranasal
Delivery Of Insulin Exhibits
Pharmacokinetic Advantages for
the Prandial Delivery of Insulin
in Human Clinical Trials.
(November 1-2, 2007).
Invited Speaker, Drug Delivery
2007,
San Diego, CA. Update on
Clinical Development of
Intranasal Peptide Therapeutics:
Results from Phase 1 Clinical
Trials with Intranasal Insulin.
(June 6-8, 2007).
Drug Delivery Partnerships,
Las Vegas, NV. Intranasal drug
delivery: challenges and
solutions through formulations
and drug devices. (January 24,
2007).
EuroTIDES,
Hamburg, Germany. Development of
a non-invasive intranasal
insulin, an alternative to
injectable insulin (December 6,
2006).
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