RedHill Biopharma Ltd 6-K, filed Sep 9, 2020

UNITED STATES SECURITIES AND EXCHANGE COMMISSION Washington, D.C. 20549

Form 6-K

Report of Foreign Private IssuerPursuant to Rule 13a-16 or 15d-16of the Securities Exchange Act of 1934

For the month of September 2020 Commission File No.: 001-35773

REDHILL BIOPHARMA LTD. (Translation of registrant's name into English)

21 Ha'arba'a Street, Tel Aviv, 6473921, Israel (Address of principal executive offices)

Indicate by check mark whether the registrant files or will file annual reports under cover of Form 20-F or Form 40-F. Form 20-F [ X ]      Form 40-F [   ]

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):

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):

Attached hereto and incorporated by reference herein is the following:

Exhibit 1: Registrant's press release entitled: “RedHill to Present at the Morgan Stanley Annual Global Healthcare Conference and Additional September Events”

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), on May 23, 2018 (Registration No. 333-225122) and on July 24, 2019 (File No. 333-232776) and its Registration Statements on Form F-3 filed with the Securities and Exchange Commission on February 25, 2016 (Registration No. 333-209702), on July 23, 2018 (File No. 333-226278) and on July 24, 2019 (File No. 333-232777).

SIGNATURES

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.

EdgarFiling EXHIBIT 1

RedHill to Present at the Morgan Stanley Annual Global Healthcare Conference and Additional September Events

TEL AVIV, Israel and RALEIGH, N.C., Sept. 09, 2020 (GLOBE NEWSWIRE) -- RedHill Biopharma Ltd. (Nasdaq: RDHL) (“RedHill” or the “Company”), a specialty biopharmaceutical company, today announced that RedHill’s Chief Executive Officer, Dror Ben-Asher, will present at the Morgan Stanley Annual Global Healthcare Conference, on Thursday, September 17, 2020.

Morgan Stanley Virtual 18^th^ Annual Global Healthcare Conference (Sept. 14-18) Fireside chat and Q&A: Thursday, September 17, 2020 Time: 8:45 a.m. EDT Speaker: Dror Ben-Asher, Chief Executive Officer

The Company will also present and hold one-on-one meetings at several additional events in September:

The Sixth Annual PharmaVOICE 100 Celebration Bioforum Panel Presentation: Thursday, September 10, 2020 Topic: Developing Clinical Trial Outsourcing Strategies that Scale as Biotechs Do Time: 12:10 a.m. EDT Speaker: Guy Goldberg, Chief Business Officer

The Wall Street Investor Forum Presentation: Thursday, September 10, 2020 Time: 11:40 a.m. EDT Speaker: Dror Ben-Asher, Chief Executive Officer

H.C. Wainwright 22^nd^ Annual Healthcare Conference (Sept. 14-16) Presentation and Q&A: Wednesday, September 16, 2020 Time: 10:00 a.m. EDT Speaker: Guy Goldberg, Chief Business Officer

Healthtech Leaders Virtual Partnering & Investment Conference (Sept. 15-18) Presentation: On-demand Speaker: Guy Goldberg, Chief Business Officer

Sachs 20^th^ Annual Biotech in Europe Forum (Sept. 21-24) Presentation: On-demand Speaker: Guy Goldberg, Chief Business Officer

Panel: Virtual Therapeutic Strategies to Prevent & Treat COVID-19 Date: Monday, September 21, 2020 Time: 10:00 a.m. EDT/4:00 p.m. CET Speaker: Gilead Raday, Chief Operating Officer

All presentations will be broadcasted live and available via replay for 30 days on the Company's website: https://ir.redhillbio.com.

About RedHill Biopharma RedHill Biopharma Ltd. (Nasdaq: RDHL) is a specialty biopharmaceutical company primarily focused on gastrointestinal diseases. RedHill promotes the gastrointestinal drugs, Movantik^®^for opioid-induced constipation in adults^1^, Talicia^®^ for the treatment of Helicobacter pylori (H. pylori) infection in adults^2^, and Aemcolo^®^ for the treatment of travelers’ diarrhea in adults^3^. RedHill’s key clinical late-stage development programs include: (i) RHB-204, with a planned pivotal Phase 3 study for pulmonary nontuberculous mycobacteria (NTM) infections; (ii) opaganib (Yeliva^®^), a first-in-class SK2 selective inhibitor targeting multiple indications with a Phase 2/3 program for COVID-19 and Phase 2 studies for prostate cancer and cholangiocarcinoma ongoing; (iii) RHB-104, with positive results from a first Phase 3 study for Crohn's disease; (iv) RHB-102 (Bekinda^®^), with positive results from a Phase 3 study for acute gastroenteritis and gastritis and positive results from a Phase 2 study for IBS-D; (v) RHB-107, a Phase 2-stage first-in-class, serine protease inhibitor, targeting cancer and inflammatory gastrointestinal diseases and is also being evaluated for COVID-19 and (vi) RHB-106, an encapsulated bowel preparation. More information about the Company is available at www.redhillbio.com.

This press release contains “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995. Such statements may be preceded by the words “intends,” “may,” “will,” “plans,” “expects,” “anticipates,” “projects,” “predicts,” “estimates,” “aims,” “believes,” “hopes,” “potential” 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’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 as well associated with (i) the initiation, timing, progress and results of the Company’s research, manufacturing, preclinical studies, clinical trials, and other therapeutic candidate development efforts, and the timing of the commercial launch of its commercial products and ones it may acquire or develop in the future; (ii) the Company’s ability to advance its therapeutic candidates into clinical trials or to successfully complete its preclinical studies or clinical trials or the development of a commercial companion diagnostic for the detection of Mycobacterium avium subspecies paratuberculosis (MAP); (iii) the extent and number and type of additional studies that the Company may be required to conduct and the Company’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’s therapeutic candidates and Talicia^®^; (v) the Company’s ability to successfully commercialize and promote Movantik^®^, Talicia^®^ and Aemcolo^®^; (vi) the Company’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 and sustain its own marketing and commercialization capabilities; (viii) the interpretation of the properties and characteristics of the Company’s therapeutic candidates and the results obtained with its therapeutic candidates in research, preclinical studies or clinical trials; (ix) the implementation of the Company’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 commercial products 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’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’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 on March 4, 2020. 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.

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^1^ Full prescribing information for Movantik^®^ (naloxegol) is available at: www.Movantik.com.  ^2^ Full prescribing information for Talicia^®^ (omeprazole magnesium, amoxicillin and rifabutin) is available at: www.Talicia.com. ^3^ Full prescribing information for Aemcolo^®^ (rifamycin) is available at: www.Aemcolo.com.