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Biotech / Medical : Palatin (PLTN) -- Ignore unavailable to you. Want to Upgrade?


To: Claud B who wrote (48)4/26/1999 11:17:00 PM
From: topgun_06903  Respond to of 61
 
Study Finds Palatin's Leutech Provides Better Appendicitis Diagnosis

Dow Jones Online News, Monday, April 26, 1999 at 20:57

By Raymond Hennessey, Staff Reporter
NEW YORK -(Dow Jones)- A quicker and more effective method to
diagnose appendicitis may be in the offering now that a Phase III
clinical trial has shown Palatin Technologies Inc.'s Leutech infection
imaging agent to be effective.
Clinical-trial results released Monday showed that Leutech indicated
appendicitis in 91% of patients with the condition and ruled out
appendicitis in 96% of the patients who didn't have it.
Leutech was also faster to use. In 38% of patients, the time from the
injection of Leutech until the first positive image was as little as
four minutes, with the median time being eight minutes. Other methods
can take more than two hours.
Shares of Palatin (PLTN) rose 75 cents, or 13%, to close at $6.75
Monday.
Leutech is an antibody that is labeled with Technetium, an imaging
agent used in nuclear medicine. The injection binds to white blood
cells, which, in turn, travel to any area of infection in the body. A
scan after injection shows the concentration of white blood cells and,
as a result, the source of the infection.




To: Claud B who wrote (48)4/26/1999 11:18:00 PM
From: topgun_06903  Respond to of 61
 
Part II

Using white blood cells has been a blessing in allowing for more
accurate diagnoses of patients with appendicitis, but there have been
drawbacks to traditional methods, said Dr. Samuel Kipper, assistant
professor of radiology at the University of California, San Diego, and a
member of the nuclear medicine department at Tri-City Medical Center in
Oceanside, Calif.
Under current methods, technicians draw blood from a patient,
separate the white blood cells, label them with the imaging agent, then
reinject the blood cells back into the patient. The process can take
more than two hours, said Kipper, who worked on the Leutech trial.
Hospitals also run the risk of injecting the patient with another
patient's blood under the old method, Kipper said. "It doesn't happen
often, but it can happen," he said. "If you're dealing with several
patients at once, there is that risk."
With Leutech, no patient needs to have blood taken, so it saves time
and eliminates the risk. In addition, the quality of the images is the
same as found in traditional blood-cell methods, Kipper said.
For appendicitis patients, Leutech could lead to a reduction in
unnecessary surgeries, said Dr. Eric Rypins, professor of surgery at the
University of California, Irvine, and chief of general and vascular
surgery at Tri-City.
When patients with severe abdominal pain go to an emergency room,
about 50% immediately can be diagnosed with appendicitis and referred to
surgery, while the other half need a closer look.
Most of the latter patients are admitted for observation, then
re-evaluated later. Traditionally, doctors were taught that "the best
test for appendicitis is the test of time," Rypins said.
Once doctors do decide to operate, the rate of unnecessary operations
is often between 15% and 20%, Rypins said. Tri-City Medical Center,
after screening patients using Leutech, reduced its rate to about 3%, he
said.
There were also cost savings, mostly from those patients who would
normally have been admitted for observation, but later sent home without
surgery, Rypins said. In a study of 49 patients, Rypins said Leutech
saved the hospital $20,000.
Both Rypins and Kipper said they see Leutech's use being expanded to
other inflammations and infections in the body. "This can be used for
infection imaging in general," Kipper said. "I'd use it for acute
abdominal pain, inflammatory bowel disease. (Appendicitis) kind of looks
like the tip of the iceberg."
Doctors will have to wait a bit before they can even use it to
diagnose appendicitis, though. Princeton, N.J.-based Palatin has a
meeting scheduled on May 20 with the Food and Drug Administration and
expects to apply for a biologics license application in July, said
Edward Quilty, the company's Chairman and Chief Executive.
Quilty agreed with the doctors that appendicitis was just a first
step toward other indications. Already, 19 of 45 patients have been
enrolled in a Phase II trial using Leutech to diagnose osteomyelitis, or
an infection of the bone, Quilty said.
But Palatin expects so-called off-label usage - usage of a product by
doctors for indications not specifically approved by the FDA - once
Leutech is approved, Quilty said. Leutech could be on the market within
a year after its files its application, though Quilty said the company
plans to ask for an expedited review.
In the meantime, Palatin is still working on finding a marketing
partner for Leutech. Palatin is in the "late stages" of talks with an
unnamed large imaging company and a final deal could be announced in the
next 30 to 45 days, Quilty said.
- Raymond Hennessey; 201-938-5240;
raymond.hennessey@dowjones.com
Copyright (c) 1999 Dow Jones & Company, Inc.
All Rights Reserved.

Posted: 04/26/99, 10:40PM E



To: Claud B who wrote (48)11/5/2001 12:26:56 PM
From: Skywatcher  Respond to of 61
 
Walter Reed Army Medical Center Seeks Palatin Technologies' LeuTech for Potential Early Detection of
Inhaled Anthrax Infection
PRINCETON, N.J.--(BW HealthWire)--Nov. 5, 2001--Palatin Technologies, Inc. (AMEX: PTN - news) announced today that it has teamed with the Walter Reed Army Medical Center, Washington, D.C. to evaluate the clinical utility of Palatin's investigational infection imaging and diagnostic product, LeuTech®, for the early detection of inhalation anthrax.
Under the agreement, made through The Henry M. Jackson Foundation for the Advancement of Military Medicine, Inc., study patients exposed to anthrax will begin receiving LeuTech® scans this week. LeuTech® is a radiolabeled monoclonal antibody that binds to white blood cells that collect at sites of infection, thus enabling the infection to be easily and rapidly imaged and detected with a gamma camera.
Carl Spana, Ph.D., president and chief executive officer of Palatin said, ``We are excited to be collaborating with Walter Reed Army Medical Center in this clinical evaluation of LeuTech®, and consider it a privilege to assist the U.S. government in the fight against bioterrorism. Historically, inhalation anthrax infection has been almost uniformly fatal because of the difficulty in recognizing the disease early and its rapidly progressive clinical course. We believe the diagnostic quality, speed, and the ease of use of LeuTech® represent key advantages over other technologies for the imaging and diagnosis of infection. Based on these advantages, we are optimistic that LeuTech® has the potential to diagnose infection with inhalation anthrax in the early stages of the disease process, when it is most likely to be treatable.''
In the early stages of infection with inhalation anthrax, bacteria multiply in the lymph nodes in and around the lungs. White blood cells migrate to these localized areas of bacterial growth to fight the invading organisms, thus offering the opportunity for LeuTech® to bind to these cells and detect the bacterial infection at an earlier stage. Diagnosing inhalation anthrax infection in its early stages, before the bacteria can poison the body with its toxins, allows patients to receive aggressive antibiotic therapy at a time when it is most effective, potentially avoiding the later-stage complications of the disease.
The initial study is being conducted at the Walter Reed Army Medical Center and will enroll up to 500 individuals believed to be at risk of having inhaled anthrax spores. ``We are excited to have LeuTech® as part of our anthrax prophylaxis study, a key objective of which is to define and validate a logical imaging protocol for the detection of early acute pulmonary anthrax infection in patients with a credible exposure to anthrax who are asymptomatic,'' said Dr. Robert Bridwell of the Walter Reed Army Medical Center.
Should the initial results of this clinical trial demonstrate LeuTech's® utility in the diagnosis of inhalation anthrax, Palatin will initiate discussions with the FDA to provide LeuTech® to other medical institutions under the regulatory provision of a Treatment IND (Investigational New Drug Application). Treatment INDs permit unapproved products to be made available to patients before general marketing begins to treat serious or life-threatening diseases or infections.
``Anthrax infection is now the latest addition to our clinical development plan for LeuTech® which targets the medical need for improved diagnosis of acute and chronic infections, including appendicitis, osteomyelitis (bone infection), post-surgical infections and bowel infections/inflammation,'' said Perry Molinoff, MD, executive vice-president of Research and Development at Palatin Technologies. ``We received a unanimous vote from the FDA Medical Imaging Drugs Advisory Committee's (MIDAC) that LeuTech® is safe and effective for the diagnosis of equivocal appendicitis, and recently reported positive interim Phase 2 clinical trial results for LeuTech® in the diagnosis of osteomyelitis. At the request of the FDA and in order to resolve manufacturing and process validation issues, we are working very closely with our manufacturer and Mallinckrodt, a subsidiary of Tyco Healthcare, to gain marketing approval of LeuTech® as expeditiously as possible.''

Hey Claud...you still there...been a LONG time.
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