
For
over twenty years, New York Oncology Hematology
has participated in clinical trials and
has played a pivotal role in the FDA approval
process of 24 new anticancer drugs. We are currently collaborating with
leading pharmaceutical and biotechnology
companies working with chemotherapy,
immunotherapy, and stem cell transplantation.
We
have a unique research infrastructure that
includes a dedicated research staff and a
standardized Institutional Review Board
approval process. This highly efficient
organization helps speed drugs from the
research lab into patient care, as quickly as
possible while providing the highest quality
care to our patients.
NYOH
participates in Phase I/II and III
clinical trials. Trials include all major
solid tumor types, hematologic malignancies
and supportive care.
Our US Oncology affiliation provides us
with a robust panel of clinical trial options
for our patients. We also participate in
National Cancer Institute (NCI) sponsored
research through the Eastern Cooperative
Oncology Group (ECOG), and
the National Surgical Adjuvant Breast
and Bowel Project (NSABP).
The
End
of
Cancer
Begins
with
Research.
CURRENT
OPEN CLINICAL TRIALS AT NYOH:
Why
Do Research?
Research improves the current state of cancer
care by finding better ways to prevent and
treat cancer.
Research improves the quality of life and
extends survival for all who are diagnosed
with cancer.
Research provides patients access to new,
potentially more effective therapies which are
not otherwise available.
What Are Clinical Trials?
Clinical trials are research studies that
involve people.
These studies occur after laboratory and
animal testing has been completed.
Clinical trials are the only way new cancer
treatments can be tested for efficacy and
safety before being made available to the
public.
Each study tries to answer specific scientific
questions and find better ways to prevent,
diagnose, or treat cancer.
Why Are Clinical Trials Important?
Cancer affects us all.
Every 25 seconds a man, woman or child
in the
U.S.
is diagnosed with cancer.
About 556,500 Americans are expected to die
from cancer this year – more than 1,500
people a day.
Clinical trials contribute to knowledge and
progress against cancer.
Today’s standard treatments are based on
previous clinical trial results.
Because of progress made, many people with
cancer are living longer.
In addition to improved survival rates, clinical
trials have contributed to:
Lower
recurrence rates for many cancers
New
treatment approaches for cancers that had no
effective therapy
Fewer
side effects and better quality of life
The more people that participate in clinical trials, the
faster we can answer critical research
questions that will lead to better treatments.
Cancer
Clinical Trial Participation
Only about 3% of adult cancer patients take
part in clinical trials.
Over 80% of children
with cancer participate in clinical trials.
Why do so many children participate?
•
Trials
are considered standard of care in pediatric
oncology.
Result: Cure rates for childhood cancers now
exceed 75%.
Types
of Cancer Clinical Trials
Treatment trials involve new investigational
treatments such as new anticancer drugs.
Prevention trials involve new approaches to
prevent cancer or prevent a recurrence of
cancer.
Screening trials investigate the best way to
diagnose cancer, especially in the early
stages.
Quality-of-life/cancer control trials explore
ways to improve the comfort and
quality-of-life of cancer patients.
The
Protocol: A Trial’s Action Plan
A protocol specifically outlines the study’s
purpose.
Defines the study size and number of
participants.
Describes the plan of care and collection of
data.
Carefully developed / reviewed by the
Principal Investigator and the sponsoring
organization.
Reviewed and approved by an Institutional
Review Board (IRB).
Ensures that trial procedures are consistently
carried out.
Institutional
Review Board (IRB)
IRBs review that:
Risks to participants are minimized
Risks are reasonable in relation to
anticipated benefits
Selection of participants is equitable
Informed consent is sought for each
participant
Informed consent is appropriately documented
Data collection is monitored to ensure safety
Privacy and confidentiality are protected
Why
consider a Clinical Trial?
- Alternative to standard treatment
- May provide early access today to the
treatments of tomorrow
- Monitored very closely even after the
treatment is completed
- Only through clinical trials do we learn to
prevent, better treat, and cure cancer AND
help others in the future!
For
further information on clinical trials, please
contact us at these locations:
NYOH
- Albany
NYOH
- Latham
400 Patroon Creek Blvd., Suite 1
1003 Loudon Rd.
Albany, NY 12206
PO Box 610
(518) 489-0044
Latham, NY 12110
Michele Butler, Research Manager
(518) 786-3122
Kathy Disisto, Research Coordinator
NYOH
- Albany Medical Center
NYOH
- Rexford
43 New Scotland Ave
896 Riverview Rd.
Albany, NY 12208
Rexford, NY 12148
(518) 262-6696
(518) 399-4600
Joanna Walsh, Research Coordinator
Darlene Pafundi, Research Coordinator
NYOH
-Amsterdam
NYOH - Troy
1700 Riverfront Center
2200 Burdett Ave., Suite 106
Amsterdam, NY 12010
Troy, NY 12180
(518) 843-0020
(518) 272-2097
Laura Marion, Research Coordinator
Mary Bowen, Research Coordinator
NYOH
- Hudson
69 Prospect Ave.
Hudson, NY 12534
(518) 822-8484
Joanne Wagman, Research Coordinator

In
2006, New York Oncology Hematology was the proud recipient of
two national prestigious awards:
American
Society of Clinical Oncology (ASCO) Community
Research Award
and
US
Oncology “Outstanding Growth in Accruals”
For
more information on clinical trials,
please visit www.clinicaltrials.gov
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