SI
SI
discoversearch

We've detected that you're using an ad content blocking browser plug-in or feature. Ads provide a critical source of revenue to the continued operation of Silicon Investor.  We ask that you disable ad blocking while on Silicon Investor in the best interests of our community.  If you are not using an ad blocker but are still receiving this message, make sure your browser's tracking protection is set to the 'standard' level.
Biotech / Medical : Peregrine Pharmaceuticals, Inc.( PPHM)
PPHM 4.220+0.7%Jan 5 4:00 PM EST

 Public ReplyPrvt ReplyMark as Last ReadFilePrevious 10Next 10PreviousNext  
To: Terry D. who started this subject3/10/2004 7:41:09 PM
From: cjgaddy   of 3795
 
PR 3-10-2004: Epstein's "TNT3/IL-12" in H.Hybridomics

No question, this TNT3/IL12 thrust has CHINA and MERCK/Germany written all over it:

1. "This work was supported in part by Cancer Therapeutics, Inc. (Los Angeles, CA) and MediBiotech, Inc. (Los Angeles, CA)." ... Abstract authors: Li J, Hu P, Khawli LA, Yun A, Epstein AL.

2. "The TNT technology platform for the delivery of cytokines is currently under development by Merck KGaA of Darmstadt, Germany under a licensing agreement with Peregrine (http://www.peregrineinc.com/prelease.asp?id=140130628).

3. Recall EL in the 12-20-2001 CC: "What I do know is Medipharm is really focused on our TNT, variations of the Vasopermeation Enhancement, and TNT delivery of Cytokines".

4. From the 8-13-2003 China Approval PR: "Medipharm plans to start clinical testing in China of two new antibody based drugs in 2004. ...To date, the TNT technology platform has been used to deliver various killing agents such as radioactive isotopes, cytokines, chemokines and liposomes to solid tumors."

Reminder: Terry has uploaded THE FULL Adobe-Reader PDF of EPSTEIN's Feb2004 Hybrid Hybridomics "chTNT-3/huIL-12" article to the Peregrine Palace. Go to groups.yahoo.com and select GALLEY-PROOF.

Now, today's PR:

"Peregrine Announces Publication of Data Related to its Tumor Necrosis Therapy Technology Platform"
peregrineinc.com

Tustin, CA – March 10, 2004 - Peregrine Pharmaceuticals (NASDAQ:PPHM) announced today the publication of an article in Hybridoma and Hybridomics related to its Tumor Necrosis Therapy (TNT) technology platform. The research article describes the expression and testing of a TNT monoclonal antibody linked to the human cytokine Interleukin 12 (IL-12). The expressed fusion protein retained functional activity and induced a 44% reduction in prostate tumor growth in therapy experiments. The TNT technology platform for the delivery of cytokines is currently under development by Merck KGaA of Darmstadt, Germany under a licensing agreement with Peregrine.

Cytokines are immune system stimulators that help the human body fight infection and disease. Monoclonal antibodies are targeting agents that recognize specific structures and can be used to deliver therapeutic agents. The combination of a targeting antibody linked to a cytokine is known as an immunocytokine. In the newly published article, an immunocytokine was constructed using a TNT antibody linked to the cytokine IL-12. The TNT antibody guides IL-12 to the tumor where the cytokine can help boost the body’s ability to fight the cancer. Immunocytokines are expected to have lower side effects than conventional chemotherapy and thus represent an attractive alternative to standard tumor therapy.

About Tumor Necrosis Therapy (TNT):
Rapidly growing tumors quickly outgrow their blood supply resulting in a region of tumor cells that do not receive adequate oxygen, nutrients and waste removal. The accumulation of dying cells results in the formation of a dead, or necrotic, core present in virtually all solid tumors beyond a very small size. TNT based products directly target and bind to dead and dying tumor cells found in virtually all solid tumors. Hence, TNT-based therapeutic agents have the potential to deliver therapeutic agents preferentially targeted to virtually all solid tumors.

Peregrine’s TNT antibodies bind to universal intracellular antigens, DNA/Histone complexes, exposed in the necrotic core of malignant solid tumors. Since DNA and Histone are not normally accessible in normal tissues, the DNA/Histone complex represents a stable and specific marker of tumors

Given TNT's near universal appearance as a tumor marker, TNT antibodies make excellent delivery molecules for a wide variety of anti-cancer killing agents. To date, the TNT technology platform has been used to deliver various killing agents such as radioactive isotopes and cytokines to solid tumors.

About Peregrine Pharmaceuticals:
Peregrine’s research and development efforts focus on discovering and developing products that effect blood flow to tumors. Peregrine’s vascular research programs fall under several different proprietary platforms including Anti-Phospholipid Therapy (APT), Vascular Targeting Agents (VTAs), anti-Angiogenesis, and Vasopermeation Enhancement Agents (VEAs). The company has research collaborations with pharmaceutical and biotechnology companies to develop its VTA platform for therapeutic and diagnostic applications and expects to enter its first APT compound into clinical trials for cancer therapy during calendar year 2004.

Peregrine’s vascular agents may also have applications in other angiogenesis-dependent diseases besides cancer such as diabetes, arthritis, skin disorders and eye diseases. Peregrine currently has exclusive rights to over 80 U.S. and foreign patents and patent applications that broadly cover its vascular programs. In addition, the company is currently evaluating its proprietary targets for use in treating non-angiogenesis dependent diseases such as viral infection. The company believes that the pre-clinical data generated by the company and the broad nature of its intellectual property will provide many opportunities for product development, partnering and licensing.

Peregrine’s most clinically advanced therapeutic program is based on a targeting platform outside vascular biology. This technology platform is known as Tumor Necrosis Therapy (TNT) and targets dead or dying tumor cells that are common to the majority of different tumor types. Cotara, the most clinically advanced TNT program, is currently in a phase I clinical trial for the treatment of colorectal carcinoma at Stanford University Medical Center. In addition, we have received protocol approval from the U.S. Food and Drug Administration (“FDA”) to initiate a registration clinical study for the treatment of brain cancer. The company is currently seeking a development or funding partner to move the brain cancer program forward. The company believes that continuing the clinical development of Cotara in tumor types other than brain cancer will add significant value to the program. The company has a research collaboration to develop immunocytokines based on the TNT platform and a TNT based agent has been developed and approved for the treatment of lung cancer in China under a licensing agreement. <snip>
Report TOU ViolationShare This Post
 Public ReplyPrvt ReplyMark as Last ReadFilePrevious 10Next 10PreviousNext