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RESEARCH COLLABORATION AGREEMENT ON RX-0201 CLINICAL DEVELOPMENT

Collaboration Agreement

RESEARCH COLLABORATION AGREEMENT ON RX-0201 CLINICAL DEVELOPMENT | Document Parties: Rexahn Corporation | REXGENE Biotech Co. You are currently viewing:
This Collaboration Agreement involves

Rexahn Corporation | REXGENE Biotech Co.

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Title: RESEARCH COLLABORATION AGREEMENT ON RX-0201 CLINICAL DEVELOPMENT
Governing Law: Maryland     Date: 3/31/2006

RESEARCH COLLABORATION AGREEMENT ON RX-0201 CLINICAL DEVELOPMENT, Parties: rexahn corporation , rexgene biotech co.
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Exhibit 10.5

 

RESEARCH COLLABORATION AGREEMENT

ON RX-0201 CLINICAL DEVELOPMENT

 

This RESEARCH COLLABORATION AGREEMENT ON RX-0201 CLINICAL DEVELOPMENT (the "Agreement") is entered into between Rexahn Corporation, a company based in the United States, carrying on business at 9700 Great Seneca Highway, Rockville MD 20850 USA ("REXAHN ") and REXGENE Biotech Co., Ltd., located at 1330-13 Seocho-Dong, Seocho-Gu, Seoul, Korea ("REXGENE"). REXAHN and REXGENE are collectively referred to as "Parties" and individually referred to as "Party" in this Agreement.

 

WHEREAS , REXAHN has developed a certain proprietary therapeutic compound for the treatment of cancer denominated as RX-0201;

 

WHEREAS , REXGENE is engaged in the development of pharmaceutical products; and,

 

WHEREAS , the Parties are interested in pursuing collaborative research and development efforts regarding RX-0201;

 

NOW THEREFORE , in consideration of the mutual promises contained herein, and for other good and valuable consideration, the receipt of which is hereby acknowledged, REXGENE and REXAHN agree as follows:

 

1


 

1.

 

DEFINITIONS

 

 

1.1

Licensed Technology shall mean technology relating to REXAHN Product RX-0201, including all Improvements resulting from research and development efforts pursuant to this Agreement.

 

 

1.2

Licensed Patents shall mean all United States and foreign patents presently or in the future issued that cover Licensed Technology, including continuation, divisional, reexamined and reissued patents, issuing or claiming priority, either directly or indirectly, from pending United States Provisional Application No. 60/404010 filed August 16, 2002.

 

 

1.3

Licensed Products shall mean any and all drug products, including those incorporated in combination products, which consist of, include or in anyway incorporate the Licensed Technology.

 

 

1.4

Improvements shall mean all improvements, developments, discoveries and inventions that relate to the Licensed Products.

 

 

1.5

Net Sales shall mean all gross revenues, derived from sales, minus commissions, sales taxes, shipping, and insurance costs.

 

 

1.6

Territory shall mean all countries in Asia .

 

2.

COLLABORATIVE RESEARCH & REGISTRATION EFFORTS

 

 

2.1.

The Parties shall cooperate fully to develop a research and development plan for the purpose of registering RX-0201 for sale and use in the Republic of Korea ("Korea") and in other countries within the Territory. The research and development plan shall include, at a minimum, clinical and animal trials to be conducted in the United States, clinical trials to be conducted in Korea and other Asian countries, and the exchange of data derived from such trials .

 

2


 

 

2.2.

REXAHN shall provide, as its initial contribution to the joint development and research, a License to the Licensed Technology for the purpose of permitting research and development by REXGENE.

 

 

2.3.

REXGENE shall provide, as its initial contribution to the joint development and research, One Million Five Hundred Thousand Dollars (US $1,500,000) to be used by REXAHN in the further development of RX-0201.

 

 

2.4.

The Parties will each contribute those efforts necessary to perform the agreed upon research and development tasks. Specifically, REXGENE will conduct the clinical trials necessary for registration of Licensed Products in Korea and other countries in the Territory. REXGENE will bear its own expenses and costs in connection with these activities. REXAHN will conduct those animal and clinical trials in the United States or otherwise outside the Territory on RX-0201.

 

 

2.5.

The Parties will share data derived from any research and trials without further fees.

 

 

2.6.

REXGENE will be responsible for, and bear the expense for, all registration and other approvals in connection with the use or sale of Licensed Products in Korea and other countries in the Territory.

 

3


 

 

2.7.

REXAHN will prosecute all patent applications and bear all costs outside of the Territory. REXGENE will prosecute all patent applications and bear all costs within the Territory, but, REXAHN will undertake to prosecute patent applications for the Licensed Technology in Korea, Japan, China and India.

 

 

2.8.

Both Parties agree to share any Improvements and to provide all assistance necessary to pursue additional patent rights arising from such Improvements.

 

 

2.9.

REXGENE and REXAHN will have the License Rights described in Section 2 of this Agreement.

 

3

GRANT OF LICENSE

 

 

3.1

REXAHN agrees to grant and does hereby grant to REXGENE an exclusive license within the Territory, with right to sublicense, to employ the Licensed Technology to make, have made, use, sell, and import Licensed Products.

 

 

3.2

REXGENE agrees to grant and does hereby grant to REXAHN an exclusive license everywhere outside the Territory, with right to sublicense, to employ the Licensed Technology to make, have made, use, sell, and import Licensed Products.

 

4.

ROYALTIES

 

 

4.1

REXGENE agrees to pay REXAHN a royalty of three percent (3%) of Net Sales of Licensed Products in


 
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