UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549

 

FORM 8-K

  

CURRENT REPORT

Pursuant to Section 13 or 15(d) of the

Securities Exchange Act of 1934

Date of Report (Date of earliest event reported): December 8, 2014

  

Immune Therapeutics, Inc.

(Exact name of registrant as specified in its charter)

 

Florida 000-54933 59-3226705
(State or other jurisdiction (Commission (IRS Employer
or incorporation) File Number) Identification Number)
     

  

37 North Orange Avenue, Suite 607, Orlando, Florida 32801
(Address of principal executive offices) (Zip Code)

  

(888) 613 - 8802

(Registrant’s telephone number, including area code)

  

Not Applicable

______________________________________________

Former name or former address, if changed since last report

  

Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions ( see General Instruction A.2. below):

 

Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)

 

Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)

 

Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))

 

Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))

  

1.01 Entry into a Material Definitive Agreement.

 

On December 8, 2014, we entered into a Contract for the Compounding of Pharmaceutical Products (the “ Agreement ”) with KRS Global Biotechnology, Inc. (“ KRS ”) pursuant to which KRS will carry out the services of compounding, packaging and distributing tablets of our low dose naltrexone product in accordance with the Agreement.

 

The Agreement has an initial term of three years starting on December 8, 2014. The parties may agree to extend the initial term for one year. KRS will pay us for every tablet it compounds, packages and sells, calculated in accordance with a formula set forth in the Agreement. We represented and agreed, among other things, (i) to provide sales and marketing assistance necessary to allow KRS to fulfill its obligations, (ii) that the rights provided to KRS in the Agreement to provide our low dose naltrexone product are exclusive only to KRS and will not be provided to any other party during the term of the Agreement, (iii) to provide KRS with specifications for raw materials and the necessary technical specifications for the compounding and packaging processes of our low dose naltrexone product, as available, (iv) in the event the Agreement is terminated by us for any reason, to reimburse KRS for all unused packaging materials, (v) in the event that KRS does not receive and ship at least 1,000 orders (prescriptions), to reimburse KRS for 100% of the “ramp up costs” of compounding our product, even in the case where we cancel/terminate the Agreement, (vi) to assign a person from us, agreeable to both parties, to be in charge of communication between us and KRS, and (vii) to provide the design of secondary packing and instructions in any language we need.

 

We also agreed that under our authorization and our patents, KRS must order and have shipped directly to KRS the active pharmaceutical ingredient necessary for the production of our low dose naltrexone product and KRS shall submit a purchase order to us for such active pharmaceutical ingredient. We agreed to pay such purchase order directly to the supplier of the active pharmaceutical ingredient. Upon KRS receiving a minimum of 10,000 orders (prescriptions) per month, KRS will pay for the active pharmaceutical ingredient for each such 10,000 orders month.

 

The Agreement is filed as Exhibit 10.1 to this Current Report on Form 8-K and is incorporated herein by reference. The foregoing description of the material terms of the Agreement and the transactions contemplated thereby does not purport to be complete and is qualified in its entirety by reference to such exhibit.

 

Item 9.01 Financial Statements and Exhibits.

 

(d) Exhibits.

 

Exhibit No. Description of Exhibit
   
10.1 Contract for the Compounding of Pharmaceutical Products, dated December 8, 2014

 

 

 

SIGNATURE

 

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.

 

  Immune Therapeutics, Inc.
     
    By: /s/ Noreen Griffin
    Noreen Griffin, Chief Executive Officer

 

Date: December 15, 2014

 

Exhibit 10.1

 

CONTRACT FOR THE COMPOUNDING OF PHARMACEUTICAL PRODUCTS

 

This CONTRACT FOR THE COMPOUNDING OF PHARMACEUTICAL PRODUCTS (this “Agreement”) is hereby entered into this 8th day of December, 2014, by and between Immune Therapeutics, Inc., a company organized and currently existing in good standing under the laws of the State of Florida and formerly known as TNI BioTech, Inc. (“TNI”); and KRS Global Bio Technology, Inc., a company organized and currently existing in good standing under the laws of the State of Florida (“KRS”). TNI and KRS are sometimes hereinafter referred to individually as a “party” and/or collectively as the “parties”.

 

WHEREAS , TNI has developed a pharmaceutical product designed to enhance the immune system and treat various diseases, including lymphoma, HIV virus/AIDS, Kaposi Sarcoma, Lymphoma, Ovarian Cancer, Epithelial, Germ Cell Tumor, Low Malignant Potential Tumor, Crohn’s Disease, Prostate Cancer, Irritable Bowel Syndrome, Pancreatic Cancer, Pancreatic Neuroendoctrine Tumors, Parkinson’s disease, multiple sclerosis, and herpes. This product is composed of the active drug naltrexone hydrocholoride and can be commercialized in the form of a tablet, capsule, or as a cream. The product is called LDN. TNI has all of the proprietary and legal rights to LDN. The form of this drug can be modified as agreed to in writing by the parties; and

 

WHEREAS , KRS is a pharmacy that specializes in the compounding of a variety of pharmaceutical products, and has the necessary licenses and permits to compound, import and sell pharmaceutical products. At such time as TNI obtains the necessary approvals to commercialize LDN, TNI will notify KRS in a timely manner to obtain the necessary permits to produce and commercialize LDN and will provide the information and documentation for KRS to obtain these permits; and

 

WHEREAS , the purpose of this Agreement is to set out the terms and conditions under which KRS will carry out the services of compounding, packaging and distributing the LDN tablets, capsules and/or creams (the“LDN-CDS”); and

 

WHEREAS, the tablets, capsules and creams will be compounded for shipment to patients in the United States or any other areas authorized by KRS. In the compounding and packaging process, KRS must also comply with the United States of America’s Food and Drug Administration’s (“FDA”) good manufacturing practices (“CGMP”) and those of any regulatory bodies.

 

NOW, THEREFORE , FOR AND IN CONSIDERATION OF THE RECITALS/WHEREAS CLAUSES SET FORTH ABOVE, WHICH SHALL BE DEEMED AN INTEGRAL PART OF THIS AGREEMENT AND NOT MERELY RECITALS THERETO, AND FOR $10.00 AND OTHER GOOD AND VALUABLE CONSIDERATION, THE RECEIPT AND SUFFICIENCY OF WHICH IS HEREBY ACKNOWLEDGED AS RECEIVED BY EACH PARTY FROM THE OTHER, THE PARTIES AGREE AS FOLLOWS:

 

1. KRS REPRESENTATIONS AND OBLIGATIONS: KRS hereby represents and agrees as follows :

 

  A) To have all permits and licenses necessary to carry out the LDN-CDS;
B) To ship the amounts of compounded LDN ordered by physicians for their patients within thirty (30) days from the day the order is received;
C) To use only the Active Pharmaceutical Ingredients (the “ API”) and raw materials that have been previously approved by TNI and only in the amounts that have been previously indicated in writing;
D) To obtain and pay for an insurance policy that protects the raw materials that are provided by TNI and the finished LDN tablets, capsules and/or creams (the “LDN-P”) against any natural disaster, or destruction of any reasonably insurable type (the “Insurance”). The Insurance must at all times protect the goods at the market value of the inventory, finished and unfinished goods and raw materials provided by TNI from time to time, and must name TNI as an additional loss payee;
E) To allow, upon prior reasonable notice, periodic inspection of the compounding and packaging process to be carried out either by TNI directly or by an agreed to third party on behalf of TNI;
F) To order in advance and have shipped directly to KRS all API for the LDN-CDS and packaging materials for the LDN-P;
G) To ensure strict compliance with the CGMP;
  I)

To provide sufficient storage space for the raw materials, ingredients, and packaged products and to protect them from theft, flooding or vermin and spoilage and provide the aforementioned Insurance.

 

2. TNI'S REPRESENTATIONS AND OBLIGATIONS: TNI hereby represents and agrees as follows:

 

A) To provide sales and marketing assistance necessary to allow KRS to fulfill its obligations;
B) KRS and TNI agree that under the authorization of TNI and TNI’s patents, KRS shall order and have shipped directly to KRS the API necessary for the production of the LDN-CDS and KRS shall submit a purchase order for such API to TNI. TNI shall pay such purchase order directly to the supplier of the API by sending funds by wire transfer to such supplier within three (3) business days of receipt of such purchase order. Notwithstanding the foregoing, upon KRS receiving a minimum of 10,000 orders (prescriptions) per month (a “10K Month”), KRS will pay for the API for each such 10K Month;
C) The rights provided to KRS herein to provide the LDN-CDS and produce the LDN-P, are exclusive only to KRS and will not be provided to any other party or entity during the term of this Agreement;

C) To provide KRS with specifications for raw materials and the LDN -P;

D) To provide KRS with the necessary technical specifications for the compounding and packaging processes of the LDN-P, as available;
E) In the event this Agreement is terminated by TNI for any reason, to reimburse KRS for all unused packaging materials for the LDN-P, which unused packaging materials KRS will provide to TNI;
F) To pay KRS, all agreed upon amounts, in a timely manner (within 10 days of receipt of an invoice from KRS);
G) In the event that KRS does not receive and ship at least 1,000 orders (prescriptions), to reimburse KRS for 100% of the “ramp up costs” of providing the LDN-CDS and producing the LDN-P, even in the case where TNI cancels/terminates this Agreement, which provision shall survive the cancellation/termination of this Agreement (for purposes of this Agreement, “ramp up costs” are defined as all costs and expenses of labor and materials related to the testing, and required FDA and other governmental documentation/approvals of test data);
H) To assign a person from TNI, agreeable to both parties, to be in charge of communication between TNI and KRS;
I) To provide the design of the secondary packing and the instructions in any language TNI needs; and
J) To submit all marketing materials to KRS for review and approval and such marketing materials must be reviewed and approved by KRS in writing.

 

3. KRS agrees that:

 

A) The raw materials provided for the LDN-CDS are to be used strictly for the compounding and packaging process of LDN and may under no circumstance be sold, transferred, or create a lien over, unless TNI has given prior written consent for such sale, transfer or lien;
B) Under no circumstances will KRS sell a pharmaceutical product containing the same formula and technical specifications as those used to manufacture and produce LDN; and/or

C) KRS will not share, license, or otherwise transfer the formula or technical specifications for the manufacturing of LDN.

 

4. QUALITY CONTROL: TNI will have the right, upon reasonable prior notice and at TNI’s own cost and expense, to carry out quality audits or to consent through an agreed to third party to inspect the compounding and packaging processes. TNI may solicit any quality certificate from KRS that may be required by the regulatory bodies of the United States, as it relates to the LDN-P.
5. TERM. This Agreement will have an initial term of three (3) years starting on the date of execution by all parties . The parties may agree to extend the term of this Agreement for one (1) year under the same terms and conditions, which agreement shall be made in writing, and executed at least sixty (60) days before the expiration of this Agreement.

6. EARLY TERMINATION: The parties can terminate this Agreement under any of the following circumstances:

 

A) Mutual agreement, in writing,
B) Either party may terminate this Agreement if the other party fails to materially comply with any of the material obligations that are to be fulfilled hereunder. In such an event, the nonbreaching party shall give written notice of such breach and the other party shall have thirty (30) days to cure same before the termination is final. In case of early termination by TNI, KRS will return any and all raw materials, finished products, patents, documents containing technical information, and any other property that belongs to TNI and complete all existing LDN purchase orders before termination, so long as TNI simultaneously reimburses KRS for all costs, expenses and profit related to same.

 

7. PAYMENT: KRS will pay TNI for every tablet or capsule it manufactures, packages and thereafter sells, calculated in accordance with the attached Exhibit “A” Payment Terms and Conditions, which Exhibit A is incorporated into this Agreement by this reference . Reconciliation and payment for each week (ending Friday) will be made by the following Wednesday.

 

To enable TNI to reconcile amounts paid weekly in accordance with this section 7, KRS will provide TNI with the following information on a per batch basis:

 

(a) A list of all invoices evidencing shipments that occurred for the subject batch, showing the number of the tablets, capsules and/or creams that were compounded and shipped to patients, and the prices paid by patients; and

(b) A list of all shipping costs incurred by KRS to make the shipments in (a) above, together with copies of invoices or statements provided by the shipping vendor; provided, however, that if KRS receives a 10K Month, KRS will not be required to provide the information in 7 (a) and (b) above for that 10-K Month.

 

TNI shall have the right, upon reasonable prior notice and at TNI’s own cost and expense, to carry out periodic audits to verify that all amounts owed to TNI have been paid.

 

I f during the term of this Agreement, the costs for manufacturing and packaging should increase , KRS shall inform TNI in writing within no more than sixty (60) days of such increase (the “Increase Notice”), at which time both parties shall, within 10 days of the date of such Increase Notice, reach a new agreement on pricing in the form of an addendum or KRS may immediately terminate this Agreement without any further notice or cure period.

 

8. ASSIGNMENT: Neither party may , under any circumstances, assign this Agreement, either totally or partially, n or the rights contained herein without the prior written consent of the other party and the assignee’s assumption of all of the obligations of the assignor as set forth herein.

 

9. LABOR RELATIONSHIP: This Agreement does not create any type of labor relationship between TNI and the employees of KRS. Therefore, KRS and TNI will be solely responsible for paying any and all wages, indemnifications, insurance policies, or any other payment due to its employees in accordance with all labor laws, any internal regulation and any trade union agreement, if one were to exist.

 

10. NONDISCLOSURE: “Confidential Information” shall be defined as any nonpublic information disclosed by one party to the other party and shall be deemed to include the following information of the respective parties, without limitation: (a) e-mail addresses, customer lists, the names of customer contacts, the names of investor contacts, investor lists, professional contacts, business plans, technical data, product ideas, personnel, contracts and financial information; (b) patents, trade secrets, techniques, processes, business methodologies, schematics, employee suggestions, development tools and processes, computer printouts, computer programs, design and drawings and manuals, and improvements; (c) information about costs, profits, markets and sales; (d) plans for future development and new product concepts; (e) all documents, books, papers, drawings, models, sketches, graphic design, photographs, type fonts, topographical treatments and text, illustrations, visual designs, animation, sound, visual elements, prints and other data of any kind and description, including electronic data recorded or retrieved by any means, that have been or will be disclosed, as well as written or oral instructions or comments.

 

Notwithstanding the foregoing, Confidential Information of a party shall not include information that (i) has become public knowledge through legal means without fault by the receiving party, (ii) is already public knowledge prior to the disclosure of the Confidential Information by the party disclosing Confidential Information (“Disclosing Party”) to the party receiving Confidential Information (“Receiving Party”), (iii) is known to the Receiving Party prior to Disclosing Party’s disclosure of the same pursuant to this Agreement, or (iv) is independently developed by the Receiving Party without reference to or use of the Confidential Information.

 

In the performance of this Agreement or in contemplation thereof, each party and its employees and agents may have access to Confidential Information owned or controlled by the other party. All Confidential Information supplied by one party to the other shall remain the exclusive property of the party supplying same. The Receiving Party shall use a reasonable degree of care, which in any event shall not be less than the same degree of care which the Receiving Party uses to protect its own proprietary and confidential information, to keep, and have its employees and agents keep, confidential any and all Confidential Information . In keepin g therewith , the recipient shall not copy or publish or disclose the Confidential Information to others, or authorize its employees, or agents or anyone else to copy, publish or disclose it to others, without the Disclosing Party’s written approval, nor shall the Receiving Party make use of the Confidential Information except for the purposes of executing its obligations under this Agreement, and shall return the Confidential Information to the Disclosing Party at its request.

 

Without limiting the preceding paragraph, each party recognizes and acknowledges that:

(i)            the Confidential Information is a valuable, special and unique asset of the Disclosing Party and that disclosure of any confidential information would cause considerable harm to the Disclosing Party's business reputation;

(ii)          it is vital to the Disclosing Party’s legitimate business interests that (1) the confidentiality of the Confidential information be preserved and (2) the Confidential information only be used for the purpose of this Agreement;

(iii)         disclosure of the Confidential Information to any other person or entity or use of the Confidential Information by or on behalf of any other person or entity could result in irreparable harm to the Disclosing Party;

(iv)         disclosure or use beyond the permitted scope of Confidential Information entrusted to the Disclosing Party by its clients and contractors could expose Disclosing Party to substantial damages; and

(v)           Receiving Party shall not use or in any way implement the Confidential Information to compete with the Disclosing Party.

The furnishing of Confidential Information hereunder shall not constitute or be construed as a grant of any express or implied license or other right, or a covenant not to sue or forbearance from any other right of action (except as it relates to the purpose of this Agreement), by Disclosing Party under any of its patents or other intellectual property rights.

 

11. INTELLECTUAL PROPERTY RIGHTS AND USE OF INFORMATION: All

trademarks, US and foreign patents and extensions thereof, trade secrets, formulas, ideas, designs, computer software, discoveries and procedures used or disclosed by TNI in relation to the services agreed upon in th is Agreement are owned exclusively by TNI and may be used only in relation to the manufacturing and packaging processes described herein. Unless otherwise in the public domain, they may be given no other use unless there is prior written consent by TNI.

 

12. FORCE MAJEURE: For purposes of this Agreement, Force Majeure shall mean a cause or event that is not reasonably foreseeable or prevented or otherwise caused by or under the control of the party, such as floods, wars and riots. If a case of force majeure were to arise which materially affect the duties or obligations of a party, the party affected by it must inform the other party in writing of its occurrence within three (3) business days. In that case, both parties may then agree on one of the following:

 

A) To continue to carry out this Agreement under the same terms and conditions, making provision for compliance subject to the issues affected by the Force Majeure;
B) To continue to carry out this Agreement under new conditions;

C) To terminate this Agreement without any further obligations;

D) If no agreement is reached, this Agreement may be terminated by the party to whom the duties or obligations are due, after proper notice and time to cure regarding a default (as set forth in this Agreement) .

 

13. CONFLICT RESOLUTION: This Agreement shall be governed by, construed and enforced in accordance with the laws of the jurisdiction in the State of Florida. Any dispute that the parties cannot resolve through mediation must submit to arbitration. Such arbitration shall be arbitrated in Palm Beach County, Florida, whether commenced by TNI or KRS, in accordance with the applicable rules of the American Arbitration Association, Commercial Dispute Resolution Procedures, and judgment on the award rendered by the arbitrator(s) shall be binding on the parties and may be entered in any court having jurisdiction.

 

14. REVISION AND MODIFICATIONS TO THIS AGREEMENT: The parties agree to revise this Agreement, on an annual basis. Any modification that may be agreed upon must be done in writing signed by the parties and in the form of an addendum and will be considered part of this Agreement.

 

15. MISCELLANEOUS:

 

A) Subject to applicable law, this Agreement may be amended, modified, or supplemented only by a written agreement signed by parties.
B) Any failure of any party to comply with any obligation, covenant, agreement, or condition herein may be waived by the party entitled to the performance of such obligation, covenant, or agreement or who has the benefit of such condition, but such waiver or failure to insist upon strict compliance with such obligation, covenant, agreement, or condition will not operate as a waiver of, or estoppel with respect to, any subsequent or other failure. Whenever this Agreement requires or permits consent by or on behalf of any party hereto, such consent will be given in a manner consistent with the requirements for a waiver of compliance as set forth above.
C) All notices, requests, demands, and other communications required or permitted hereunder will be in writing and will be deemed to have been duly given when delivered by hand, or one day when sent overnight by a nationally recognized overnight delivery service (such as FEDEX), or two days after being mailed by certified or registered mail, return receipt requested, with postage prepaid:

 

 

   
  If to TNI: Immune Therapeutics, Inc.
37 North Orange Ave., Suite 607
Orlando, Florida 32801
    Attention: General Counsel
     
  If to the KRS: KRS Global Bio Technologies, Inc.
    791 Park of Commerce Blvd. Suite 600
    Boca Raton, Florida 33487
     
  Copy to: Bruce Jay Toland, Esq.,
    Bruce Jay Toland, P.A.
    Brickell City Tower
    80 SW 8 th Street, #2805
    Miami, FL 33130
     

 

or to such other address as the parties may furnish to each other in writing.

 

 

D) All section titles or captions contained in this Agreement are for convenience only and shall not be deemed part of the context nor effect the interpretation of this Agreement.
E) This Agreement contains the entire understanding between and among the parties and supersedes any prior understandings and agreements among them respecting the subject matter of this Agreement.
F) This Agreement shall be binding upon the heirs, executors, administrators, successors and assigns of the parties hereto.
G) In the event an arbitration is brought by any party under this Agreement to enforce any of its terms, or in any appeal therefrom, it is agreed that the prevailing party shall be entitled to reasonable attorneys’ fees to be fixed by the arbitrator and/or appellate court.
H) In computing any period of time pursuant to this Agreement, the day of the act, event or default from which the designated period of time begins to run shall be included, unless it is a Saturday, Sunday, or a legal holiday, in which event the period shall begin to run on the next day which is not a Saturday, Sunday, or legal holiday, in which event the period shall run until the end of the next day thereafter which is not a Saturday, Sunday, or legal holiday.
I) All pronouns and any variations thereof shall be deemed to refer to the masculine, feminine, neuter, singular, or plural as the identity of the person or persons may require.
J) This Agreement or any section thereof shall not be construed against any party due to the fact that said Agreement or any section thereof was drafted by said party.
K) The parties hereto shall execute and deliver all documents, provide all information and take or forbear from all such action as may be necessary or appropriate to achieve the purposes of the Agreement.
L) Nothing herein shall be construed to be to the benefit of any third party, nor is it intended that any provision shall be for the benefit of any third party.
M) If any provision of this Agreement, or the application of such provision to any person or circumstance, shall be held invalid, the remainder of this Agreement, or the application of such provision to persons or circumstances other than those as to which it is held invalid, shall not be affected thereby.

 

IN WITNESS WHEREOF, the parties hereto have executed this Agreement as of the date set forth above.

 

Immune Therapeutics, Inc.

   

KRS Global Bio Technology, Inc.

     
By: /s/ Chris Pearce   By: /s/ Ricardo Roscetti
Christopher Pearce, COO   Ricardo Roscetti, CEO
     
By: /s/ Noreen Griffin    
Noreen Griffin, CEO    

 

 

 
 

 

Exhibit “A” Payment Terms and Conditions  
   
Net Distributable Revenue Calculation (30 day supply) Without blister pack:  

 

Gross Revenue (excluding actual shipping costs)

(A)
Less API Cost .06 Per Tablet (Advanced by TNI) (B)
Less Packaging, Excipient & CC Charges (Advanced by KRS) (C)
  Box for Medication  
  Shipping Box  
  Bottle & Label  
  Excipients  
  Less Credit Card Charge @ 2.5% (calculated with shipping charge)  
   Total Per Order  
  Net Distributable Revenue (D)
   
   
Net Distributable Revenue Calculation (30 day supply) With blister pack:  

 

Gross Revenue (excluding actual shipping costs)

(A)
Less API Cost .06 Per Tablet (Advanced by TNI) (B)
Less Packaging, Excipient & CC Charges (Advanced by KRS) (C)
  Blister pack  
  Box for Medication  
  Shipping Box  
  Excipients  
  Less Credit Card Charge @ 2.5% (calculated with shipping charge)  
   Total Per Order  
  Net Distributable Revenue (D)
   
*Shipping charge of a flat $10.00 for ground will be collected and retained by KRS.    
Additional charge for overnight shipping will be determined based on patient zip code.  
   
   
TNI Reimbursement Calculation:  
API Reimbursement (B)
50% of Net Distributable Revenue (D) (D)
  Due to TNI Total of B&D