As reported  June 20, 2016, Inovio Pharmaceuticals Inc. has received Food and Drug Administration approval to begin human testing of its experimental Zika vaccine being developed to prevent Zika virus infections.

The Plymouth Meeting-based biopharmaceutical company is developing the Zika vaccine in a partnership with GeneOne Life Science Inc. of Seoul, South Korea. The two companies are also working with academic collaborators from the United States and Canada with whom they have previously collaborated to advance Inovio’s Ebola and MERS vaccines into clinical development.

In preclinical testing the synthetic Zika vaccine induced robust antibody and T cell responses in small and large animal models, demonstrating the product’s potential to prevent Zika infections in humans.

Dr. J. Joseph Kim, the president and CEO of Inovio (NASDAQ: INO), said as of May 2016, 58 countries and territories reported continuing mosquito-borne transmission of the Zika virus, justifying development of a Zika vaccine.

“The incidences of viral infection and medical conditions caused by the virus are expanding, not contracting,” Kim said.

Inovio expects to dose its first subjects for phase-I clinical trials, which will test the Zika vaccine candidate in 40 health volunteers, within the next few weeks at multiple sites including Philadelphia. The company’s plan is to report interim results later this year.

No Zika vaccine or therapy currently exists for the Zika virus.

The Zika virus was first identified in Uganda. It is classified as a flavivirus— a family of viruses including yellow fever, dengue, and West Nile virus, which are introduced to people through mosquito bites.

Because the Aedes species of mosquitoes that spreads Zika virus is found throughout the world, health officials are concerned that Zika will continue to spread to new countries and regions. Zika can also be sexually transmitted.

The most common symptoms of Zika virus are fever, rash, joint pain, and conjunctivitis.

The virus has also been linked to a severe birth defect called microcephaly which arises from infection during pregnancy. Microcephaly is a rare condition marked by an abnormally small head and incomplete brain development.

Zika is also associated with Guillain-Barré syndrome, which causes muscle weakness of the limbs and in severe cases may cause almost total paralysis including the inability to breath.

No vaccine or therapy currently exists for the Zika virus. (1)

The science behind a depopulation agenda

Recently, a company called INOVIO has been given a $45 million contract by DARPA, the research arm of the Dept of Defence, to pursue Ebola vaccines and the methods of delivery. They were also given a $28 million grant by the N.I.H.

http://www.fiercevaccines.com/story/inovio-led-team-picks-24m-darpa-develop-ebola-vaccine-treatments/2015-09-22

The company has been given awards for a new start up company, but, this company has a long history with links to government agencies, pioneers of DNA technology and many Pharmaceutical companies.

Reported as being a new start up company.

And yet has been involved in the Industry since 2000 http://www.economist.com/node/17258858

Curiously, no mention of Inovio in the VGX history, although it clearly states that the company was created by Kim and Weiner.

http://vgxii.com/about/history/

Alarming New Research in Genetic Engineering

In the beginning, Dr Joseph Kim created a partnership with his University professor. Professor Weiner was a pioneer of genetically modified DNA. He was also heavily involved in HIV and is a pioneer.
(It should be noted that soon after Polio experimental vaccines were given to tens of millions in Africa, during the 50,s and 60s, coincides with when HIV first began.)

These researchers began in 2000 as VGX Pharmaceutical Inc manufacturing plasmid DNA. They had three failed trials in three years. They then worked with Advisys which was an animal lab. They used their new DNA technology for creating a synthetic Porcine growth hormone for Pigs.

This enabled them to increase the breeding age of pigs and was soon taken up by the farming industry.

Using PCV2 which is Porcine Circovirus, they are able to use their new technique called Electroporation for the first time, they were pioneers in the animal health division.

During this time, the swine flu vaccine patent was first filed, in 2005,which was not patented untill 2009, just 5 months after this was patented, swine flu was being rolled out as the next pandemic.

(Many companies were involved and the WHO and other agencies proclaimed a full blown pandemic when none existed, Baxter were also fined for allowing the Swine flu virus to be contaminated within the vaccines.)

Dr Kim has openly stated that his company has many of his friends and colleagues on the scientific board and on the board of directors.
He was employed by Merck who paid for his Phd and now boasts having people such as the former President of Merck , Adel Mahmoud, on his board, Morton Collins, who served as technology policy advisor to President G.H.W Bush and former Senior Vice president of of Merck, Ford Hutchinson as a scientific advisor who is also a Wellcome trust advisor and was involved in many controversial drugs like Gardasil and Rotateq.

Rotateq was licensed in 2006 and found to contain both PCV1 and PVC2 and Rotarix which was manufactured by GSK in 2008 was found to contain PVC1.

Both of these vaccines were found to have contained PCV in 2010, years after they had been first given the go-ahead by the FDA. Both were also suspended when the evidence came to light only to be re-instated as safe two months later.

Curiously an online medical search engine called Medworm, which informs details of medical resources and data, published this information on the day that the FDA suspended the vaccines. The writer of that Information was Dr Joseph Kim.

http://www.medicineandtechnology.com/2010/03/fda-stop-using-rotarix-vaccine-until-we.html?utm_source=feedburner&utm_medium=feed&utm_campaign=Feed%3A+mdjosephkim+%28Medicine+and+Technology%29

The fact that this man had his PhD paid for by his friends at Merck, has serious implications to ethics. Such an arrangement gives him a free hand with no ethical, moral questions, that works both ways. They wont pester him and he will do what is expected of him.

At this point it should be noted that the FDA had failed to spot the pig DNA in the initial tests, but then, had also deemed it safe to carry on with this vaccine.

Where was the enquiry asking how pig DNA could find its way into vaccine that were supposed to be for diarrohea?

Given that PCV2 is a post weaning multi system wasting disease which was an emerging diseases of swine/pigs, how could the FDA even know how safe it was?

Given that this was the exact PCV that Dr Kim was working on, maybe someone should be asking him these question?

It cannot be denied that he was aware of this development, given that it was he, who informed the world of the FDA decision on the very day that the FDA announced this.

At this point, I would like to turn your attention to his partner, Dr Weiner. An advisor to GSK, Pfizer and other Pharma giants, he is also a special employee and advisor to the FDA and the NIH grant review process. (Did he influence the decision by the FDA to allow the contaminated vaccines to be used and classified as safe?)

No wonder then, how Inovio was given a 28 million dollar grant by the NIH to develop its genetically modified DNA based monoclonal antibodies and its new process of electroporation.

This is the process by which the very first genetically modified virus was used in this case, it was on pigs.

https://gdsajj.wordpress.com/tag/dna-vaccines/

In 2006 VGX were providing HIV vaccines in Africa.

In 2008, VGX, which is also owned by Inovio, went into an arrangement to manufacture DNA plasmid for human use.

In 2009, Inovio filed a IND with FDA to start trials on humans with a DNA vaccine for H5N1.

Their lead drug for Swine flu was licensed in 2009.

https://en.wikipedia.org/wiki/H5N1_clinical_trials

In 2010, 8 different plasmids were produced in a study provided by the Defence threat Reduction Agency of the DoD.

In 2011 they were working with Homeland security on Foot and mouth disease.

New strains of foot and mouth disease began in 2012 in USA.
Under a research and development agreement, they were working with US Dept of homeland security and Plum Island Animal disease centre.

This does not sound like a company that should be getting awards for a new start up company!

So now they have been given the go ahead to produce not only the ebola vaccines but also the new novel method to administer them.
Here is were we have to get a bit scientific minded, but bear with me.
THE METHOD

Electroporation

This is a pulsed electrical current applied to local tissue to allow the cell to have holes in it to allow just enough synthetic DNA to enter, then the pulse stops and the cell closes, the problem here is that according to studies, a manuscript in Molecular therapy with references from 74 separate articles written in 2004, concludes that the use of gene transfer using electroporation should only be used with human antibodies because problems could arise from cancer to death.

http://www.researchgate.net/publication/8375091_Therapeutic_Antibody_Gene_Transfer_An_Active_Approach_to_Passive_Immunity

Recombinant DNA encompasses only one area of genetic engineering; namely, Biospecific biochemical and microbiological to alter,relatively controlled and reasonably predictable manner, the molecules that encode the genetic characteristics of an organism, and to introduce specifically selected new set of genetic Instructions.

The specific molecular manipulations that are made and the exact methods used to make them can vary widely from one recombinant DNA experiment to another. The basic process,usually involves the Initial isolation or synthesispecific set of chemically identical nucleic acid molecules (usually molecules are then bonded…?) specially prepared vector (carriers) that usually are plasmids. bacteriophages, or other virus-like infectious entities that can self-replicate in appropriate host cells. After the bonding has been completed, the modified can be inserted into bacteria or other cells that have been prepared biochemically to accept them. If the vectors have been “constructed” appropriately, the piece of initially selected DNA can give the recipient new genetic instructions. For Instance, the host cell might be given the capability to synthesize an enzyme that it previously could not make.

This science is exactly what you would need for a population reduction ‘PROGRAM’ using ‘mandated’ vaccine legislation! Poisoning the well i.e. GMO food could also work well with this science achieving population reduction quotas.

https://gdsajj.wordpress.com/2009/11/29/h1n1-h2n2-h3n2-and-h5n1-combo-dna-influenza-vaccine-ready/

Dr Kim has also served his five year tenure as a member of the Global Agenda Council of the World Economic Forum, which is clearly a huge advocate of a one world global government, attended by the world,s top 1000 corporations and involves a network of Government leaders.
There is also a curious question, why is there a Fox news interview with Dr Kim in which he stated that his company would have the human tests for an Ebola vaccine trialled in Jan 2015?

http://video.foxnews.com/v/3849677626001/pharmaceutical-companies-racing-to-develop-ebola-vaccine/?playlist_id=2694949841001#sp=show-clips

Wen in his August 2015 speech to shareholders, he claimed that his new Ebola vaccine would be used in human trials in the next eighteen months or sooner?

http://www.inovio.com/assets/000/000/002/456.pdf

If this man has the capability to create synthetic viruses which they intend to inject into peoples cells to create an immune response, what would happen if the same synthetic virus was put into a vaccine and injected into the blood?

Would the body then react as though it was fighting a real virus, thus creating the cytokine storm that is the very thing that would cause death or symptoms of Ebola?

We were informed via the mainstream media that the only way to test for Ebola was for those tests to be sent to UK/US labs,giving the power to inform the numbers of people infected, to the World Health Organisation and other Govt agencies in the West.

And yet, a new piece of equipment which has just recently been promoted as a breakthrough for testing Ebola, with a small mobile unit, that allows those tests to be achieved in minutes, appears to have been known and available since 2009!

A story appeared in a local Scottish paper, a few days ago, it claimed that a new technique to test Ebola in minutes had been perfected except the truth is that this technology was created by this company and Wellcome Trust in 2006.

http://www.heraldscotland.com/news/13950478.Scots_scientist_s_Ebola_testing_kit_rolled_out_in_West_Africa/

They had the means to test people in minutes when they started this new range of products in 2009.

Why has it been suppressed?

http://www.samedanltd.com/directory/detailed/687

It was part created by Wellcome trust, who are heavily involved in the genetics agenda being played out.

I think the evidence gathered here brings a lot of scientific, military, bio-companies and government organisations into question on ethics and also on their real agenda.

What exactly is the real Agenda?

Why are scientists tampering with the building blocks of existence?

According to this report, geneticists are using XNA, which is foreign, unknown and unnatural DNA which could be passed onto future generations.

http://augmentinforce.50webs.com/XNA-%20ARTIFICIAL%20LIFE-ARTIFICIAL%20INTELLIGENCE%20or%20ALIEN%20LIFE-ALIEN%20INTELLIGENCE.htm#XNA-%20ARTIFICIAL%20LIFE-ARTIFICIAL%20INTELLIGENCE%20or%20ALIEN%20LIFE-ALIEN%20INTELLIGENCE

Genetic information storage and processing rely on just two polymers, DNA and RNA which is being tampered with to include XNA.

The European Commission has supported the Integrated Project PACE in its Future Emerging Technologies program from 2004-2008.

http://cordis.europa.eu/ist/fet/

is the final public report of results and experience in PACE.—PACE has created the foundation for a new generation of embedded IT using programmable chemical systems that approach artificial cells in their properties of self-repair, self-assembly, self-reproduction and evolvability

http://ec.europa.eu/index_en.htm

According to scientists, XNA could lead to different forms of life on other planets or could be used to create new synthetic forms of life.

This technology is now being used in vaccinations with no regulations or oversight and can only lead to a mutation of the human race, is this what pandemics are really all about?