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J_U_ICE
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It seems the labeling and packaging is all set hopefully news this week on patent confirmation www.xechemnigeria.org

NICOSAN™
350mg
NICOSAN™
Products under development


NICOSAN™
250mg
NICOSAN™
Products under development





In July, 2002, Xechem acquired an exclusive, worldwide license to develop NICOSAN™ (HEMOXIN™ in the US) from the Nigerian government and, subsequently, received U.S. orphan drug status for HEMOXIN™ from the FDA in August, 2003. The product is made from four botanical species indigenous to Nigeria. NICOSAN™ is produced there today by Xechem. The Company expects to launch NICOSAN™ in Nigeria’s 4,000,000 SCD patient market, the world’s largest SCD market, in 2005. SCD, a devastating hereditary blood disorder characterized by acute painful crisis, organ damage, anemia and early death, affects over 80,000 African Americans in the U.S. alone. Based on published data and human experience, the Company believes the successful clinical development of HEMOXIN™ represents an unusually low risk. In phase II human studies in Nigeria, published in Phytomedecine, HEMOXIN™ was shown to be safe in all patients and effective in approximately 80% of patients. As published in the May 2003 issue of the British Journal of Hematology, Asakura and colleagues from Children’s Hospital of Philadelphia (CHOP) and the University of Pennsylvania demonstrated the anti-sickling effects of HEMOXIN™ in transgenic mice. This lends significant credibility to the Nigerian human experience to initiate clinical trials in the U.S.



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JL
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I donno is the pump team running XKEM ready?
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topsail
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I think the pump team went on vacation. Sure wish they'd come back soon, PPS keeps walking down.
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J_U_ICE
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I wish they would come back to I'm sick of waiting for a run

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J_U_ICE
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INTERESTING READ

Xechem Pharmaceuticals [XKEM.OB]is in an interesting position
here.They have a Sickle Cell treatment called Nicosan/Hemoxin,the
only effective treatment for Sickle Cell Disease in the world other
than the highly toxic chemo drug made by BMS called
Hydroxyurea.Nicosan/hemoxin is a combination of 4 herbs indiginous to
the jungles of Nigeria in Africa.Xechem's production facility in
Abuja,Nigeria is very close to being completed & ready for production
of Nicosan.They are presently awaiting word from the Nigerian drug
agency NAFDAC for approval of Nicosan.Lets back up.Nicosan is made
from a combination of 4 herbs..so is it a drug or a herbal treatment?
It's both actually.We believe very strongly that NAFDAC will approve
Nicosan anyday now as a "drug" but what about the FDA & marketing the
product in the U.S.?If Nicosan is marketed in the U.S. as a herbal
treatment they do not need the blessing/approval from the FDA for
starters.The FDA approval process for a "drug" can take as long as 6-
8 years & cost up to 800 million dollars.In other words it would be a
long,long,long time before Nicosan was available in the U.S.as a drug
to treat Sickle Cell disease.That's the catch.The FDA says this: only
a "drug" can cure disease.So the answer to getting Nicosan/Hemoxin
into the U.S. market? Yep.. as a "herbal treatment" for Sickle Cell
Disease.No need for approval from the FDA.No 6-8 years of
harassment,setbacks & everyother roadblock the FDA would surely set
up to block the approval of Nicosan to protect the sales of Bristol-
meyer,Squibb's Hydroxyurea.Yes I know how the FDA works...so as of
right now Xechem Nigeria website is up [& there is a order form that
can be filled out to order Nicosan online directly from the webpage
[its not working as Nicosan is still not available... yet].Sales in
the U.S. could begin as soon as production starts...remember as long
as you don't make any claims that Nicosan cures anything it can be
sold in the U.S. as a "herbal treatment"you can say it is for SCD but
we don't claim Nicosan does anything...you know how it works..health
food stores etc....Nicosan does not cure SCD anyway.It supresses the
symptoms of the horrible disease.In test studies 90% of patients
achieved significant pain reduction & moreover 73% of the patients
achieved TOTAL REMISSION from the disease after just 6 months of
Nicosan therapy.Now you are wondering how does Xechem protect Nicosan
as a herbal treatment?That is where the lawsuit that Xechem won last
year over BMS is so very important.Xechem proved that they held the
rights to the herbal Cancer treatment "Paciltaxel" that BMS stepped
all over & violated their patent by making the synthetic Cancer
drug "Taxel"..the judge in the case agreed with Xechem & awarded them
4.2 million.The money is not important...what is very important is
that BMS tried to copy Xechem's herbal Cancer treatment & lost.So if
any big pharmaceutical company was to copy Nicosan
synthetically,Xechem's legal council would simply show a judge the
verdict from the Taxel-Paciltaxel case from 2005 & the judge would
rule in Xechem's favor.Judges go by previous identical lawsuits to
make there verdicts 99% of the time.So if Xechem sells Nicosan in the
U.S.as a herbal treatment,it would be protected by that BMS-Xechem
Taxel verdict IMO. NIPRD, a Nigerian agency holds the patent for
Nicosan/Hemoxin & that would offer additional protection.Xechem says
once they get approval from NAFDAC they will begin selling Nicosan
immediately & I believe they can sell Nicosan thru their website all
over the world eventually including the u.S. market.The only country
that presented a problem was the U.S. & by selling it as an herbal
treatment that is no longer a problem.Now here is the good
part.XKEM.OB is currently at .012 a share.The chairman & CEO of
Xechem says that sales of Nicosan in Nigeria alone,should be in
excess of $500,000,000 a year.There are an estimated 12 million
people in Africa that suffer from SCD.Using Dr Pandeys $$$
figures,just Africa represents 1.7 billion in Nicosan sales per year
as Nicosan needs to be taken continually to be effective.XKEM.OB has
882 million O/S.That would give XKEM a share price of $1.93 per share
if you figure revenue from sales just in Africa.Sales will be limited
to start as the production facility in Abuja is only big enough to
supply Nigeria in the very beginning... until the 8.2 million
production facility build out is complete.

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J_U_ICE
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another interesting post from IHUB


Hey Gang,

I just spent about 15 minutes on the phone with Steve Burg. He was returning my call from yesterday prior to when I called Howard. Great conversation - Best yet by far.

We discussed why no PR on the new factory/web site.. He told me that the NICOSAN application is the largest event EVER to be placed in front of NAFDAC. 95% of all drugs used by Nigerians are imported. NICOSAN would become the LARGEST drug ever to be produced and distributed in Nigerian. He also said that the factory also needs to be approved by NAFDAC. Both the drug formula and the commercialization/development of the drug are before NAFDAC as we speak. This air a very complicated process, and a lot of politics are involved with this. Pandey is working hard every day to get this done. THE COMPANY IS AFRAID TO ISSUE ANY PR'S RIGHT NOW, BECAUSE THEY DON'T WANT TO UPSET/DISTURB NAFDAC IN ANYWAY. THE PROCESS IS SO SENSITIVE, AND NIGERIA HAS COMPLETE AND 100% CONTROL. Any screw up by XKEM, could cost dearly. No PR until final approval.

We also discussed the financing and dilution issues. No more shares have been issued, and the company is VERY CLOSE to signing a deal with UPS which Steve said is 100% not dilutive. They are doing everything possible right now to preserve shareholder value, and eliminate future dilution. The loan from UPS would support expansion of the plant in Nigeria as well as ongoing cash flow requirements until sales prop up. HE TOLD ME THAT XKEM IS REARING TO GO, AND READY TO START BLASTING OUT SALES AS SOON AS APPROVAL IS GRANTED.

We also discussed the fact the XKEM has completed testing in other parts of the world to find out where these plants can be grown outside of Nigeria. They have identified several regions in India where these plants can be grown, and have begun looking into the possibility of setting up a manufacturing facility outside of Nigeria as well.

AS FAR AS THE Q2 SALES DISCUSSED IN THE 10K. STEVE FEELS THAT THIS IS A GOOD TIME FRAME, AND EXPECTS APPROVAL ANY DAY.

The company has remained in quite period right now, because they do not want to create any adverse reactions from NAFDAC. When approval is finally granted. Look out. The PR campaign will be a machine and unstoppable.

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BULListic
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XKEM getting a lot of hits this morning? Up to 125x126 on 95% buys, perhaps the big news on the Nigerian Express is near.

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I may be wrong, but I don't think so....

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J_U_ICE
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quote:
Originally posted by BULListic:
XKEM getting a lot of hits this morning? Up to 125x126 on 95% buys, perhaps the big news on the Nigerian Express is near.

I was going to post on this but was too busy/lazy to search for the thread Thanks BULListic. caught this on IHUB last Night:


XKEM, check this out..........

Folks, I'm tellin ya's... I can't believe how BIG this is, that an Official Nigerian web site "NATIONAL DATA CENTER
FOR SCIENCE & TECHNOLOGY" now states... "5. Commercialization of Pharmaceutical Research and Development Results: A major landmark in this direction is the successful development of the sickle cell drug, NICOSAN."

This is NOT a pump BUT this is HUGE!!!!!!

http://www.nadcest.gov.ng/news/ministry.htm

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J_U_ICE
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Another IHUB post

I had a great conversation with Steve Burg yesterday afternoon. First I asked him about previous pr's and he said he doesn't have them in front of him. Frankly I didn't push it because to me they are in the past. Then I asked him if phase 3 has been done in Nigeria and he said absolutely. He said they are going to redo it again later, but will have no affect on drug getting approved. The next question was financing. He said they are still working on conventional financing, but also have a group in place to do equity financing. He said if they go with the equity financing, it will be a lot better than it has been. Steve said they don't need as much money now, because they are so close to getting cash flow. I told him that in my opinion there is no way Nigeria won't approve the drug. He said he would be shocked if it didn't go through. He said Nigeria has a lot riding on this also. He said Dr Pandy left last night to be in Nigeria for the next week. He is hoping they will get updated when Pandy is there. We talked about pricing in Nigeria and he said they haven't set a price exactly yet. I mentioned 15. - 20. dollars per month and he said that is probably the range. I said do you expect to get at least 2 million people using it right away, and he said yes, that should be about right. At 20 per month that is almost 500 million per year. Than he said that even though the United States has only about 80,000 with the disease, he expects it to be worth a lot because they will be able to charge a lot for the drug here, like in the thousands per year. He said it will be a reimbursible treatment from health insurance. He said he has been to Nigeria and see how much good the drug does. He said it is amazing. Do your own dd and this is jmo, but I am not selling now.

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topsail
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J_U_ICE: Thanks for posting what you've found out. I've tried contacting Xechem by email, but so far no response. You answered most of my pressing questions, so thanks. Good to see some movement, been stagnant for too long.

GLTA

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J_U_ICE
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Way too long but when it hits it will be huge. The company doesn't put out PR unless it is substantial which is great. I'm so sick of the BS PR like USXP

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J_U_ICE
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2x volume green day nice change of pace. Maybe it's a sign of things to come

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J_U_ICE
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The chart is set up for this to move, crazy after hours volume!!!!!! this is ready to run!!!!!!!!!!

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UVCLRules
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Time to Rock the Casbah!
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J_U_ICE
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AMERICAN BULLS BUY CONFIRMED
XKEM

XECHEM INTL INC
Daily Commentary


Our system posted a BUY CONFIRMED today. The previous SELL recommendation was issued on 05.05.2006 (4) days ago, when the stock price was 0.0118. Since then XKEM has gained 13.56% .


The recent bullish formation leading to the BUY-IF signal is confirmed today. The market seems ready for a new bullish move. Though the market opened lower today, the day’s activity created a white candlestick that closed above the previous close. This is a valid confirmation criterion.

The significant failure of the previous SELL signal is unfortunately confirmed too. Our shot went away this time. It is a fact that such signal failures are more unlikely for higher rated stocks, but it is not possible to deal with all the vagaries of the stock market. The signal system, however, continues to do an excellent job in the overall, despite such failures. This can be seen easily with a quick glance to the signal history table.

We hope that you bought this stock and still have the chance to profit from the later phase of the bullish attack. Today your important benchmark was the previous close. You were supposed to watch the session carefully, feel its bullish tendency despite the lower opening, and go long after making sure that the prices stay over the previous close.

If you bought, continue to hold this stock until the confirmation of the next SELL-IF signal. You are on relatively safe grounds as long as the future prices continue to trade above the benchmark price and if an emergency warning is not issued. What to do if you did not buy? Maybe, you did not have time to follow the session or you simply delegated the delicate job of confirmation to us. Well, it is a bit late, but not too late. You may still find suitable prices for buying in the following sessions and still profit in case of a sustained bullish move.

The market is currently cold for short-sellers. Avoid any short sales and cover the short positions immediately if there are any. We erred significantly on the short side last time, but we are sure that you may easily cover your losses (if any) by basing your future trades on our signal system.





BUY
CONFIRMED


0.0134
+0.0014 +11.67%

Candlestick Analysis
Today’s Candlestick Patterns:
White Candlestick




Today a White Candlestick was formed. This represents normal buying pressure

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J_U_ICE
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I think this is set up to move

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topsail
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Volume has picked up, but not much movement. Still glad to see interest picking up though. Hopefully we'll have an announcement soon stating the approval has been made, the factory is ready and revenue will commence.

GLTA

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i got some shares today...I think this stock will be hot for June...

I picked some cheap shares up during the dip today...going to wait til June when they launch their product...I truly believe this will be big.

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topsail
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J_U_ICE: I see your on the RSHN board as well. Own any other pennys? I'm holding RSHN, XKEM and IGTG. I'm holding them all long, although I may sell a few shares of XKEM when it pops to cover my investment. In your talks with XKEM, was there any mention of concerns with the current political climate in Nigeria?
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J_U_ICE
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quote:
Originally posted by topsail:
J_U_ICE: I see your on the RSHN board as well. Own any other pennys? I'm holding RSHN, XKEM and IGTG. I'm holding them all long, although I may sell a few shares of XKEM when it pops to cover my investment. In your talks with XKEM, was there any mention of concerns with the current political climate in Nigeria?

Topsail, sorry it took me so long to get back to you. I have flip RSHN a couple of times for some nice coin. Now I'm riding mostly free shares but I'm in for the long-term. My only other long-term pennies are XKEM BIGN and VNBL. The XKEMconversations I've posted were taken from another poster on a different message board. I was just getting out all the info I had found. Sorry for the mixup

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this one getting alot of talk from the other boards.
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THE DEVELOPMENT OF NICOSAN TM/HEMOXIN TM
A DRUG FOR THE MANAGEMENT OF SICKLE CELL DISEASE.
7.0 HISTORICAL BACKGROUND
NICOSANTM/HEMOXINTM (formerly NIPRISAN) is a drug first developed by the
National Institute for Pharmaceutical Research and Development (NIPRD) for
the management of Sickle Cell Disease (SCD). It consists of a mixture of
extracts from four tropical plants some of which are cultivated and others
found in the wild both within and outside Nigeria.
The story of NICOSANTM/HEMOXINTM will be incomplete without acknowledging
some of the great minds, which have contributed immensely towards its
development. Historically, a similar remedy was mentioned in the book titled
“Iwosan” published by the late Dr. Odumosu at the turn of the century.
However, the modern day origin of what later became patented as NIPRISAN
was due to the late Rev. Paul Ogunyale, then Pastor of the First Baptist Church
in Ibadan, Oyo State, Nigeria, who brought the attention of Prof. Charles
Wambebe, former Director General, NIPRD in late 1992 to a herbal recipe of
the drug.
From 1992 to 2001, Prof. Wambebe and his team of researchers at NIPRD,
supported by the Federal Government of Nigeria (FGN) and the World Health
Organization (WHO), worked tirelessly to develop NIPRISAN as a potent drug
for the management of SCD and was patented in the United States of America
under the leadership of Prof. Wambebe. After the retirement of Prof. Wambebe
from NIPRID, his successor, Dr. Uford S. Inyang continued tirelessly with more
developmental work in taking NIPRISAN to a higher level.
7.1 THE BIRTH OF NICOSANTM/HEMOXINTM
In August 2001, a joint conference on biotechnology was organized at Cook
College, New Brunswick, NJ between the Sheda Science and Technology
Complex (SHESTCO), Abuja and Rutgers University under the leadership of Dr.
Soji Adelaja, who was then Dean of Research at Cook College and New Jersey
Agricultural Experiment Station (Cook/NJAES), and Dr. Albert Ayeni, then Weed
Scientist at Cook/NJAES and currently Coordinator of International Programs of
Cook/NJAES.
Dr. Ramesh C. Pandey, Chairman & CEO, Xechem International, Inc.,
represented his company at this conference. What transpired during and after
the conference propelled Dr. Pandey to explore the possibilities in the
applications of biotechnology for drug production in Nigeria. At the instance
of Prof. Turner T. Isoun, the Honourable Minister of Science and Technology,
Dr. Pandey visited Nigeria for the first time in October 2001 with Dr. Albert
Ayeni. This visit aroused in Dr. Pandey the interest in exploiting biotechnology
for drug development in Nigeria. The first product of interest, NIPRISAN was
thus, introduced to him by Dr. Ayodele Coker, the Director- General of
SHESTCO, and later by Dr. Uford S. Inyang, the Director- General of NIPRID.
1
In July 2002, negotiations were successfully concluded between NIPRD and
Xechem International under the direction of Prof. A. B. C. Nwosu, then the
Honourable Minister of Health. Xechem International was granted the exclusive
rights for development, production and marketing of NIPRISAN. To give effect
to the agreement, Xechem Pharmaceuticals Nigeria Ltd, which is located within
the premises of the Sheda Science and Technology Complex, was incorporated
in 2002.
7.2 ABOUT SICKLE CELL DISEASE:
Sickle cell Disease is a genetic blood disorder caused by an abnormality in the
hemoglobin molecule as depicted in the figure below. The condition causes the
production of abnormal hemoglobin that contains portions that stick together
after the release of oxygen. This phenomenon produces stiff, sickle shaped red
blood cells that do not flow freely through blood vessels. These sickle shaped
cells create clogs in the blood vessels, which prevent the flow of normal
hemoglobin and oxygen round the body. The result is severe pain or “crises”,
ulcers, organ and tissue damage and breakdown, which eventually lead to
stroke and acute chest pain. The body’s immune system also attacks and seeks
to destroy the abnormally shaped cells, often leaving the body with an
insufficient number of normal oxygen- carrying red blood cells, which in turn
results in anemic condition that manifest in fatigue and enhanced susceptibility
to infection. It is estimated that there are 10 million sufferers of SCD
worldwide, of which about 4 million are Nigerians.
Sickle Cells Normal Cells
Repeated crisis can also result in damage to the kidneys, lungs, bones, eyes
and the central nervous system. The most feared complication for children
with SCD is a stroke which affects infants as young as 18 months. Many
children with SCD do not survive infancy or early childhood. Adults with SCD
often experience a reduction in the quality of life due to severe physical
problems such as pain, Hard- foot syndrome and acute lung complications that
can result in death. Frequent episode of severe bone pain, crises and
hospitalization significantly affect the lives of these patients. It limits their
ability to participate in normal physical activities, thus retarding their social
2
and economic advancement. It also deprives them of the joy of living life to the
fullest and instills the fear of early death in them.
Before the advent for NICOSANTM/HEMOXINTM the only known cure for the
disease is a bone marrow transplant to replace defective red blood cells with
donor healthy cells. Treatment has generally consisted of supporting therapies,
which include folic acid for anemia, penicillin to prevent infections,
pneumococcal and influenza vaccination, pain killing drugs and intravenous
injection of fluids. In the United States of America, Hydroxyurea is the only
drug approved by the Food and Drug Administration (FDA) for the treatment of
SCD. It is very expensive and toxic and patients treated with hydroxyurea
exhibit severe side effects.
7.3 HOPE FOR THE SICKLERS.
NICOSANTM/HEMOXINTM is a non- toxic, phytopharmaceutical product
composed of extracts from four tropical plants, seeds, stems, fruits and
leaves. Each plant is indispensable in the manufacturing of
NICOSANTM/HEMOXINTM. Xechem Pharmaceuticals Nigeria Limited has
developed refined and standardized small- scale formulations of
NICOSANTM/HEMOXINTM for consistent production in strict compliance with the
recommended procedures and policies of the WHO.
NICOSANTM/HEMOXINTM has already undergone phase I and phase II clinical
trials conducted in Nigeria by the NIPRD. Results from the phase III trials, if
found satisfactory, will form the final basis for an application to the National
Agency for Food and Drug Administration and Control (NAFDAC) for regulatory
approval. Further laboratory testing among others have also been done at the
National Heart, Lung and Blood Institute - Sickle Cell Disease Reference
Laboratory (NHLBI-SCDR Lab) located at the Children’s Hospital, Philadelphia,
Pennsylvania, USA. The results of these trials show that
NICOSANTM/HEMOXINTM drastically reduced the degree of sickle cell formation,
and the frequency and severity of SCD crises. Liver and kidney functions
remained normal and patients gained appreciable weight. No adverse effects
were reported during the trials. These clinical studies suggest that NICOSANTM
is a safe and efficacious phytomedicine for the management of SCD. It may
have just paved the way for ending the misery and pain of millions of SCD
sufferers in Nigeria and the world at large.
Through the instrumentality of Dr. Pandey, and based on the background of
work done at the Children’s Hospital, Philadelphia (CHOP) and other published
literature in various indexed journals, on August 15th, 2003, NICOSAN™
(NIPRISAN) was granted an Orphan Drug status by the Food and Drug
Administration of the United States of America (US-FDA). The Orphan Drug
designation, entitles a company to various incentives including the waiver of
Regulatory filing fees, access to potential funding for non- clinical and clinical
research to generate required data for marketing approval, and seven years of
marketing exclusivity once approved by the FDA.
3
This was a major break- through since it was a far- fetched possibility that the
US-FDA would designate NICOSANTM (NIPRISAN) Orphan Drug status. The
Orphan Drug status has thus, added credibility and international acceptability
to NICOSANTM (NIPRISAN) as a potent drug for the management of SCD.
4

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The difference between genius and stupidity is that genius has its limits

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pay up
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From RB,
By: alexng00
15 May 2006, 12:58 PM EDT
Msg. 31490 of 31685

In addition to the feedbacks provided by Steve Burg, I called directly NAFDAC organisation this morning to get other confirmation and updates. I pick up the phone number from the NAFDAC website and reach a person within NAFDAC who provides me another number of a responsible person,I call that person and I ask her about the submission from Xechem for Nicosan, she checks the system and confirms to me that Xechem has submitted the master drug file in March, she said they submitted the Nicosan product for 250mg, and I ask her what is the status right now, and she said it' a "go far status", so I ask her what does it mean "go far" status, she says it's the product in an advanced stage for approval, then I ask her point blank, when the product will be approved please, and she says end of May. She gives me her email address and ask me to send email if I have other questions, as the quality of the phone line is not so good. I google her name and find out that she is the Director of the Registration&Regulatory approval. Guys and girls, the Nicosan product is going to be approved latest of the end of the month. Stay tuned and GLTA

--------------------
corn oil comes from corn, olive oil from olives, where does baby oil come from?

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imakmony2005
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its coming.
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BULListic
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Sure looks like a lot of accumulation here at .012 today.

--------------------
I may be wrong, but I don't think so....

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suncruiser
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Bring on the approval were ready!
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Johnwayne
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This is where I am going to begin dumping profits,
if I ever have any again. What is a good buy in price here. I know big news is coming.

--------------------
Thanks Matto. Thanks Juice.

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J_U_ICE
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I've been waiting a while with 2M shares

--------------------
The difference between genius and stupidity is that genius has its limits

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J_U_ICE
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This is starting to raise some eyebrows rumor of drug launch by months end

Post from IHUB


Xechem Nigeria is currently working to equip the laboratories and complete the construction of its state of-the-art pharmaceutical manufacturing facility. Certain laboratory and other equipment necessary for the production of NICOSAN™ have been acquired or are in the process of fabrication and Xechem expects that the plant will be ready for full-scale production by 2006. Approximately $5 million has already been invested by Xechem in the Nigerian project to date in the form of inter-company loans. Upon completion, the Xechem Nigeria facility at SHESTCO will be one of the most modern state-of-the-art research, development and pharmaceutical test, analysis and manufacturing facilities in Nigeria.

--------------------
The difference between genius and stupidity is that genius has its limits

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topsail
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Holding 750K shares. Avg price .016 I may try to pick up some more shares since I believe XKEM has a viable product and business plan, but I'm also leery of having too much into one stock.

IMO, I agree with prior sentiment the company is waiting for the drug to be approved and to also receive approval from the Nigerian government before releasing a PR.

GLTA

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imakmony2005
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should go soon.
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JimSC
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Hope we get the great pr by the first
week of June.

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topsail
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OK, I'm confused. Bid was at .011, ask .0117 Then all of a sudden Scotttrade shows 11 million shares trading at .0074

Did other sites show this? Any ideas?

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BULListic
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Had a Heart Attack myself, "lost" 3 grand there for a minute. My ScottradeElite was down (again) when that event happened, so can't tell if it was a reverse fat finger or something more sinister.

--------------------
I may be wrong, but I don't think so....

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topsail
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Actually it ended up being about 20 million shares at .0074 Gonna be interesting to see if something is up.
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