<SEC-DOCUMENT>0001171843-18-006062.txt : 20180814
<SEC-HEADER>0001171843-18-006062.hdr.sgml : 20180814
<ACCEPTANCE-DATETIME>20180814101721
ACCESSION NUMBER:		0001171843-18-006062
CONFORMED SUBMISSION TYPE:	6-K
PUBLIC DOCUMENT COUNT:		2
CONFORMED PERIOD OF REPORT:	20180814
FILED AS OF DATE:		20180814
DATE AS OF CHANGE:		20180814

FILER:

	COMPANY DATA:	
		COMPANY CONFORMED NAME:			RedHill Biopharma Ltd.
		CENTRAL INDEX KEY:			0001553846
		STANDARD INDUSTRIAL CLASSIFICATION:	PHARMACEUTICAL PREPARATIONS [2834]
		IRS NUMBER:				000000000
		STATE OF INCORPORATION:			L3

	FILING VALUES:
		FORM TYPE:		6-K
		SEC ACT:		1934 Act
		SEC FILE NUMBER:	001-35773
		FILM NUMBER:		181014975

	BUSINESS ADDRESS:	
		STREET 1:		21 HA'ARBA'A STREET
		CITY:			TEL AVIV
		STATE:			L3
		ZIP:			64739
		BUSINESS PHONE:		972-3-541-3131

	MAIL ADDRESS:	
		STREET 1:		21 HA'ARBA'A STREET
		CITY:			TEL AVIV
		STATE:			L3
		ZIP:			64739
</SEC-HEADER>
<DOCUMENT>
<TYPE>6-K
<SEQUENCE>1
<FILENAME>f6k_081418.htm
<DESCRIPTION>FORM 6-K
<TEXT>
<!DOCTYPE HTML PUBLIC "-//W3C//DTD HTML 4.0 Transitional//EN"><html lang="en-US"><head><title>EdgarFiling</title><meta content="text/html; charset=windows-1252" /><meta name="GENERATOR" content="MSHTML 8.00.7601.18094" /></head><body style="FONT-FAMILY: Times New Roman; FONT-SIZE: 10pt"><div align="center"><div style="margin-top: 3pt; margin-bottom: 12pt;"><div style="font-size: 1pt; border-top: Black 2.5pt solid; border-bottom: Black 1.1pt solid; width: 100%;">&#160;</div></div><p style="font-size: 14pt;" align="center"><strong>UNITED STATES</strong><br /><strong>SECURITIES AND EXCHANGE COMMISSION</strong><br /><strong>Washington, D.C. 20549</strong></p><p style="font-size: 14pt; text-transform: uppercase;" align="center"><strong>Form 6-K</strong></p><p><strong></strong></p><p><strong>Report of Foreign Private Issuer<br />Pursuant to Rule 13a-16 or 15d-16<br />of the Securities Exchange Act of 1934</strong></p><p>For the month of August 2018<br />Commission File No.:&#160;001-35773&#160;</p><p><strong>REDHILL BIOPHARMA LTD.</strong><br />(Translation of registrant's name into English)</p><p><strong>21 Ha'arba'a Street, Tel Aviv, 64739, Israel</strong><br />(Address of principal executive offices)</p></div><p>Indicate by check mark whether the registrant files or will file annual reports under cover of Form 20-F or Form 40-F.<br />Form 20-F [&#160;X ] &#160;&#160;&#160;&#160;&#160;Form 40-F [&#160;&#160; ]</p><p>Indicate by check mark if the registrant is submitting the Form 6-K in paper as permitted by Regulation S-T Rule 101(b)(1):<u>&#160;&#160;&#160;&#160;&#160;</u></p><p>Indicate by check mark if the registrant is submitting the Form 6-K in paper as permitted by Regulation S-T Rule 101(b)(7):<u>&#160;&#160;&#160;&#160;&#160;</u></p><p>
 <p align="justify" style="margin-left:0in; margin-right:0in;"><font style=" color: black; font-size:10pt;">Attached hereto and incorporated by reference herein is a press release issued by the Registrant entitled:&#160;<em>&#8220;RedHill Biopharma Announces Closing of $25 Million Underwritten Offering.&#8221;</em></font></p>  <p align="justify" style="margin-left:0in; margin-right:0in;"><font style=" color: black; font-size:10pt;">This Form 6-K is incorporated by reference into the Company's Registration Statements on Form S-8 filed with the Securities and Exchange Commission on May 2, 2013 (Registration No. 333-188286), on October 29, 2015 (Registration No. 333-207654), on July 25, 2017 (Registration No. 333-219441) and on May 23, 2018 (Registration No. 333-225122) and its Registration Statements on Form F-3 filed with the Securities and Exchange Commission on February 25, 2016 (Registration No. 333-209702) and on July 23, 2018 (Registration No. 333-226278).</font></p> </p><hr style="page-break-after: always;" noshade="noshade" /><p style="text-align: center;"><strong>SIGNATURES</strong></p><p>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, thereunto duly authorized.</p><table style="font-family: Times New Roman; font-size: 10pt;" border="0" width="100%" cellspacing="0" cellpadding="0"><tr valign="top"><td width="47%">&#160;</td><td width="6%">&#160;</td><td style="text-align: left;" align="center" width="47%">REDHILL BIOPHARMA LTD.</td></tr><tr valign="top"><td width="47%">&#160;</td><td width="6%">&#160;</td><td style="text-align: left;" align="center" width="47%">(Registrant)</td></tr><tr valign="top"><td width="47%">&#160;</td><td width="6%">&#160;</td><td align="center" width="47%">&#160;</td></tr><tr valign="top"><td width="47%">&#160;</td><td width="6%">&#160;</td><td style="text-align: left;" align="center" width="47%"></td></tr><tr valign="top"><td width="47%">Date:&#160;August 14, 2018</td><td width="6%">&#160;</td><td style="text-align: left;" align="center" width="47%">By: <u>/s/ Dror Ben-Asher</u></td></tr><tr valign="top"><td width="47%">&#160;</td><td width="6%">&#160;</td><td style="text-align: left;" align="center" width="47%">Dror Ben-Asher</td></tr><tr valign="top"><td width="47%">&#160;</td><td width="6%">&#160;</td><td style="text-align: left;" align="center" width="47%">Chief Executive Officer</td></tr><tr valign="top"><td width="47%">&#160;</td><td width="6%">&#160;</td><td style="text-align: left;" align="center" width="47%"></td></tr></table></body></html>
</TEXT>
</DOCUMENT>
<DOCUMENT>
<TYPE>EX-99.1
<SEQUENCE>2
<FILENAME>exh_991.htm
<DESCRIPTION>PRESS RELEASE
<TEXT>
<!DOCTYPE HTML PUBLIC "-//W3C//DTD HTML 4.0 Transitional//EN"><html lang="en-US"><head><title>EdgarFiling</title><meta content="text/html; charset=windows-1252" ><meta name="GENERATOR" content="MSHTML 8.00.7601.18094" ></head><body bgcolor="#ffffff"><p style="text-align: right;"><strong>EXHIBIT 99.1</strong></p><p style="text-align: center;"><strong>RedHill Biopharma Announces Closing of $25 Million Underwritten Offering</strong></p><p style="text-align: center;" ></p><p>
 <p align="justify">TEL-AVIV, Israel and RALEIGH, N.C., Aug.  14, 2018  (GLOBE NEWSWIRE) -- RedHill Biopharma Ltd. (Nasdaq: RDHL) (Tel-Aviv Stock Exchange: RDHL) (&#8220;RedHill&#8221; or the &#8220;Company&#8221;), a specialty biopharmaceutical company primarily focused on proprietary drugs for gastrointestinal diseases, today announced the closing of its previously announced underwritten offering of 4,166,667 American Depositary Shares (&#8220;ADSs&#8221;), each representing ten of its ordinary shares, at an offering price of $6.00 per ADS, for gross proceeds of approximately $25 million, before commissions and other offering expenses.<br ></p>  <p align="justify">Ladenburg Thalmann &amp; Co. Inc., a subsidiary of Ladenburg Thalmann Financial Services Inc. (NYSE American: LTS), acted as the sole book-running manager for the offering.</p>  <p align="justify">The Company intends to use the net proceeds from the offering, together with its existing cash and cash equivalents, to fund clinical development programs, including preparations for a second Phase III study with RHB-104 for Crohn&#8217;s disease, initiation of a pivotal Phase III study with RHB-204 for NTM, for commercial operations including TALICIA<strong><sup>&#174;</sup></strong> (<em>H. pylori</em>) launch preparations, acquisitions, and general corporate purposes.</p>  <p align="justify">The ADSs described above were issued pursuant to a shelf registration statement that was previously filed with the Securities and Exchange Commission (the &#8220;SEC&#8221;) and declared effective by the SEC on July 31, 2018. A final prospectus supplement and accompanying prospectus related to the offering was filed with the SEC and is available on the SEC&#8217;s website located at www.sec.gov. This offering was made only by means of a prospectus. Copies of the final prospectus supplement and the accompanying prospectus relating to this offering may be obtained by contacting Ladenburg Thalmann &amp; Co. Inc., Prospectus Department, 277 Park Avenue, 26th Floor, New York, New York 10172, by calling (212) 409-2000.</p>  <p align="justify">This press release shall not constitute an offer to sell or the solicitation of an offer to buy the securities described herein, nor shall there be any sale of these securities in any jurisdiction in which such offer, solicitation or sale would be unlawful prior to the registration or qualification under the securities laws of any such jurisdiction.</p>  <p align="justify"><strong>About RedHill Biopharma Ltd.:&#160;&#160;&#160;&#160;&#160; <br > </strong>RedHill Biopharma Ltd. (Nasdaq: RDHL) (Tel-Aviv Stock Exchange: RDHL) is a specialty biopharmaceutical company, primarily focused on the development and commercialization of late clinical-stage, proprietary drugs for the treatment of gastrointestinal diseases. RedHill commercializes and promotes four gastrointestinal products in the U.S.: <strong>Donnatal<sup>&#174;</sup></strong> <strong>-</strong> a prescription oral adjunctive drug used in the treatment of IBS and acute enterocolitis; <strong>Mytesi<sup>&#174;</sup></strong> - an anti-diarrheal indicated for the symptomatic relief of non-infectious diarrhea in adult patients with HIV/AIDS on anti-retroviral therapy; <strong>Esomeprazole Strontium </strong><strong>Delayed-Release Capsules 49.3 mg - </strong>a prescription proton pump inhibitor indicated for adults for the treatment of gastroesophageal reflux disease (GERD) and other gastrointestinal conditions, and <strong>EnteraGam<sup>&#174;</sup></strong> <strong>-</strong> a medical food intended for the dietary management, under medical supervision, of chronic diarrhea and loose stools. RedHill&#8217;s key clinical-stage development programs include: (i) <strong>TALICIA<sup>&#174;</sup> (RHB</strong><strong>-105)</strong> for the treatment of <em>Helicobacter pylori</em> infection with an ongoing confirmatory Phase III study and positive results from a first Phase III study; (ii) <strong>RHB-104,</strong> with positive top-line results from a first Phase III study for Crohn's disease; (iii) <strong>RHB-204, </strong>with a planned pivotal Phase III study for nontuberculous mycobacteria (NTM) infections; (iv) <strong>BEKINDA<sup>&#174;</sup></strong><strong> (RHB-102),</strong> with positive results from a Phase III study for acute gastroenteritis and gastritis and positive results from a Phase II study for IBS-D; (v) <strong>YELIVA<sup>&#174;</sup> (ABC294640),</strong> a first-in-class SK2 selective inhibitor, targeting multiple oncology, inflammatory and gastrointestinal indications, with an ongoing Phase IIa study for cholangiocarcinoma; (vi) <strong>RHB-106,</strong> an encapsulated bowel preparation licensed to Salix Pharmaceuticals, Ltd. and (vii) <strong>RHB-107 (formerly MESUPRON), </strong>a Phase II-stage first-in-class, serine protease inhibitor, targeting cancer and inflammatory gastrointestinal diseases.</p>  <p align="justify"><em>This press release contains &#8220;forward-looking statements&#8221; within the meaning of the Private Securities Litigation Reform Act of 1995. Such statements may be preceded by the words &#8220;intends,&#8221; &#8220;may,&#8221; &#8220;will,&#8221; &#8220;plans,&#8221; &#8220;expects,&#8221; &#8220;anticipates,&#8221; &#8220;projects,&#8221; &#8220;predicts,&#8221; &#8220;estimates,&#8221; &#8220;aims,&#8221; &#8220;believes,&#8221; &#8220;hopes,&#8221; &#8220;potential&#8221; or similar words. Forward-looking statements are based on certain assumptions and are subject to various known and unknown risks and uncertainties, many of which are beyond the Company&#8217;s control, and cannot be predicted or quantified and consequently, actual results may differ materially from those expressed or implied by such forward-looking statements. Such risks and uncertainties include, without limitation, risks and uncertainties associated with (i) the initiation, timing, progress and results of the Company&#8217;s research, manufacturing, preclinical studies, clinical trials, and other therapeutic candidate development efforts; (ii) the Company&#8217;s ability to advance its therapeutic candidates into clinical trials or to successfully complete its preclinical studies or clinical trials; (iii) the extent and number of additional studies that the Company may be required to conduct and the Company&#8217;s receipt of regulatory approvals for its therapeutic candidates, and the timing of other regulatory filings, approvals and feedback; (iv) the manufacturing, clinical development, commercialization, and market acceptance of the Company&#8217;s therapeutic candidates; (v) the Company&#8217;s ability to successfully promote Donnatal<sup>&#174;</sup>, Mytesi<sup>&#174;</sup> and</em> <em>Esomeprazole Strontium Delayed-Release Capsules 49.3 mg</em> <em>and commercialize EnteraGam<sup>&#174;</sup>; (vi) the Company&#8217;s ability to establish and maintain corporate collaborations; (vii) the Company's ability to acquire products approved for marketing in the U.S. that achieve commercial success and build its own marketing and commercialization capabilities; (viii) the interpretation of the properties and characteristics of the Company&#8217;s therapeutic candidates and the results obtained with its therapeutic candidates in research, preclinical studies or clinical trials; (ix) the implementation of the Company&#8217;s business model, strategic plans for its business and therapeutic candidates; (x) the scope of protection the Company is able to establish and maintain for intellectual property rights covering its therapeutic candidates and its ability to operate its business without infringing the intellectual property rights of others; (xi) parties from whom the Company licenses its intellectual property defaulting in their obligations to the Company; (xii) estimates of the Company&#8217;s expenses, future revenues, capital requirements and needs for additional financing; (xiii) the effect of patients suffering adverse experiences using investigative drugs under the Company's Expanded Access Program; and (xiv) competition from other companies and technologies within the Company&#8217;s industry. More detailed information about the Company and the risk factors that may affect the realization of forward-looking statements is set forth in the Company's filings with the Securities and Exchange Commission (SEC), including the Company's Annual Report on Form 20-F filed with the SEC </em><em>on February 22, 2018. All forward-looking statements included in this press release are made only as of the date of this press release. The Company assumes no obligation to update any written or oral forward-looking statement, whether as a result of new information, future events or otherwise, unless required by law.</em></p> </p><p>Company contact:<br >Adi Frish<br >Senior VP Business Development & Licensing <br >RedHill Biopharma<br >+972-54-6543-112<br >adi@redhillbio.com<br ><br >IR contact (U.S.): <br >Timothy McCarthy, CFA, MBA<br >Managing Director, Relationship Manager<br >LifeSci Advisors, LLC<br >+1-212-915-2564<br >tim@lifesciadvisors.com</p></body></html>
</TEXT>
</DOCUMENT>
</SEC-DOCUMENT>
