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An Introduction to
Kanglaite Injection
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Invented by famous pharmacological Prof. Li Dapeng after decades
of efforts, Kanglaite Injection (KLT) has been listed by the Chinese government
as a "State Basic Drug", a "State Basic Medical Insurance Drug" and a "State Key
New Drug". KLT has been on top of the best selling anticancer drugs in China for
recent 5 years due to its proven effectiveness.
KLT is a unique botanically sourced molecular targeted agent
prepared as a micro-emulsion for intravenous use. It is manufactured by the
state of art technology with active substance extracted from a natural herbal
plant ¡°semen coicis¡±.
KLT has the following features.
- Killing
cancer cells directly and effectively while remarkably improving patient immune
function;
- Synergistic
in increasing efficacy and in reducing toxicity when combined with chemotherapy
regimens or radiation therapy;
- Providing
high energy nutrition to treat cachexia;
- Relieving
cancerous pain markedly;
- Improving
patient quality of life and notably prolonging survival;
- With
little adverse reaction itself
In China KLT is
mainly used in the following situation.
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- Combined with
chemo regimens to minimize toxic reaction & enhance effect
- Combined with
radiotherapy to improve sensitivity
- Preoperational
monotherapy to prevent further spread and metastasis
- Monotherapy
after inefficacious chemotherapy
to elevate
KPS, MST and TTP, etc.
- Treating late
stage advanced and metastatic cases
to
elevate KPS, MST and TTP, etc.
- Controlling
cancerous pain with long lasting effect but without addiction
- Improving
cachexia
to provide
high energy nutrition
- Applied in
intervention with arterial perfusion in both large and small doses
- Eliminating
hydrothorax and pericardial effusion, etc.
Standard treatment
course for KLT is 200 ml (2 bottles) per day via intravenous drip x 42 days (84
bottles). There is a break for 4-5 days after 21 days. And clinical experiences
in China and Russia suggest 2 treatment courses for those with late stage
advanced and metastatic tumors for better therapeutic effect and evident
prolongation of life.
Based on pre-clinical studies at John Hopkins University, USA,
tumor-inhibitive rate of KLT on transplanted breast carcinoma induced by cell
strain MDA-MB-231 was over 50%. KLT could inhibit the expression of COX2 of the
strain in vitro and act as an inhibitor of fatty acid synthase. The broad
ranged basic studies in China also revealed KLT different mechanisms such as
inducing cancer cell apoptosis, inhibiting angiogenesis, reversing MDR and
regulating gene expression of Fas/Apo-1 and Bcl-2.
Both Chinese and overseas clinical experiences have shown that
KLT has proven effect in the treatment of cancers mainly at sites of lung,
breast, liver, nasopharynx, esophagus, stomach, pancreas, kidney, colon-rectum,
ovary and prostate. This agent is also applied in the treatment of malignant
lymphoma and acute leukemia. KLT has brought great benefits to over 500,000
cancer patients in more than 2,000 big or medium hospitals in China since 1997.
The year 1995 witnessed KLT patent certificates granted from
China and USA, In August 1997 the phase III clinical study was successfully
completed and the injection was officially launched in China after final
approval from the Ministry of Public Health.
FDA approved KLT clinical study in
USA in March 2001 and the phase I study at Huntsman Cancer Institute, Salt Lake
City, Utah was satisfactorily completed which laid a solid foundation for
forthcoming clinical trials. The US "Science" magazine covered the success of
KLT in China and USA in its January issue of 2003.
The whole story in PDF format
Russian Federation approved KLT clinical study in January 2002
and the phase II study was smoothly ended in April 2003 with inspiring outcomes.
In December 2003 the registration certificate was issued from Russian Ministry
of Health and KLT has been marketed in Russia from 2005 with positive response.
Currently an international multi-center randomized clinical study on KLT
combined with first line chemotherapeutic drugs in the treatment of non-small
cell lung cancer (NSCLC) is in progress.
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