Exelixis and Iconic Therapeutics Enter into Exclusive Option and License Agreement for Novel Antibody-Drug Conjugate Program

On May 16, 2019 Exelixis, Inc. (Nasdaq: EXEL) reported that it has entered into an exclusive option and license agreement with Iconic Therapeutics, Inc. (Iconic), a private biopharmaceutical company focused on cancer and retinal disease, to advance an innovative next-generation antibody-drug conjugate (ADC) program for cancer (Press release, Exelixis, MAY 16, 2019, View Source [SID1234536439]). This collaboration reflects Exelixis’ ongoing strategy to build a pipeline beyond its lead product, CABOMETYX, through both internal drug discovery and external business development. This agreement with Iconic is Exelixis’ second strategic collaboration focused on novel biologics, following the company’s collaboration with Invenra, Inc. announced in May 2018. This exclusive agreement is Iconic’s first strategic collaboration in oncology and leverages the company’s innovative Tissue Factor antibody expertise.

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This press release features multimedia. View the full release here: View Source

Under the terms of the agreement, Exelixis will gain an exclusive option to license ICON-2, Iconic’s lead oncology ADC program, in exchange for an upfront option payment to Iconic of $7.5 million and a commitment of preclinical development funding. Exelixis would exercise its option at the time of a potential IND application, and upon doing so would make an option exercise payment to Iconic and assume responsibilities for all subsequent clinical development and commercialization activities. Should Exelixis elect to exercise its option, Iconic will become eligible for future development, regulatory and commercialization milestone payments, as well as royalties on potential sales.

"Iconic Therapeutics is pursuing an innovative approach to targeting Tissue Factor, a promising target with early clinical validation and potential applicability across a wide variety of cancers," said Peter Lamb, Ph.D., Executive Vice President and Chief Scientific Officer of Exelixis. "This agreement provides Exelixis with an attractive entry into the antibody-drug conjugate space, and reflects our preference for success-based terms that reward our partners for long-term shared success. We’re looking forward to working with the Iconic team to advance this exciting program, which is complementary to Exelixis’ small molecule and emerging biologics capabilities."

ICON-2 represents a potential best-in-class program targeting TF in solid tumors. TF is highly expressed on tumor cells and in the tumor microenvironment. TF overexpression, while not oncogenic itself, facilitates angiogenesis, metastasis and other processes important to tumor development and progression. ICON-2 is a rationally designed second-generation ADC with potential for an improved therapeutic index and safety profile.

"We believe this partnership with a premier oncology company provides further validation of our novel approach," said William L. Greene, M.D., Chief Executive Officer of Iconic Therapeutics. "Exelixis’ clinical development and commercialization expertise, evidenced by the growing success of the cabozantinib franchise, make it the ideal partner as we advance this promising program towards the clinic. Iconic Therapeutics’ deep expertise in Tissue Factor biology and antibody-drug conjugate design sets the ICON-2 program apart from other approaches to this historically challenging target," Dr. Greene added.

Affimed Announces First Quarter 2019 Financial Results and Corporate Update Conference Call on May 22, 2019

On May 16, 2019 Affimed N.V. (Nasdaq: AFMD), a clinical stage biopharmaceutical company committed to giving patients back their innate ability to fight cancer, reported that it will host a conference call on Wednesday, May 22, 2019 at 8:30 a.m. ET to discuss its first quarter 2019 financial results and recent corporate developments (Press release, Affimed, MAY 16, 2019, View Source [SID1234536438]).

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The conference call will be available via phone and webcast. To access the call, please dial +1 631 510 7495 for U.S. callers, or +44 (0) 2071 928000 for international callers, and reference conference ID 1083705 approximately 15 minutes prior to the call.

An audio webcast of the conference call can be accessed in the "Webcasts" section on the "Investors" page of the Affimed website at View Source A replay of the webcast will be available on Affimed’s website shortly after the conclusion of the call and will be archived for 30 days following the call.

Verastem Oncology to Present at the 20th Annual B. Riley FBR Institutional Investor Conference

On May 16, 2019 Verastem, Inc. (Nasdaq:VSTM) (Verastem Oncology or the Company), focused on developing and commercializing medicines seeking to improve the survival and quality of life of cancer patients, reported that the Company will present at the 20th Annual B. Riley FBR Institutional Investor Conference on Thursday, May 23, 2019 at 1:30 p.m. PDT in Beverly Hills, CA (Press release, Verastem, MAY 16, 2019, View Source;p=RssLanding&cat=news&id=2398830 [SID1234536433]).

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A live webcast of the presentation will be available on the investors section of the Company’s website at www.verastem.com. An archived presentation will be available for 90 days.

TG Therapeutics Announces Data Presentations at Upcoming Medical Meetings

On May 16, 2019 TG Therapeutics, Inc. (NASDAQ: TGTX), reported the schedule of upcoming data presentations at the 55thAmerican Society of Clinical Oncology (ASCO) (Free ASCO Whitepaper) annual meeting, to be held May 31 – June 4, 2019, in Chicago, Illinois; the 24thEuropean Hematology Association (EHA) (Free EHA Whitepaper) annual congress, to be held June 13 – 16, 2019, in Amsterdam, Netherlands; and at the 15thInternational Conference on Malignant Lymphoma (ICML), to be held June 18 – 22, 2019, in Lugano, Switzerland (Press release, TG Therapeutics, MAY 16, 2019, View Source [SID1234536432]). Details of the data presentations are outlined below. 2290083

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Data to be presented at the ASCO (Free ASCO Whitepaper) meeting:

• Oral Presentation: Umbralisib monotherapy demonstrates efficacy and safety in patients with relapsed/refractory marginal zone lymphoma: A multicenter, open label, registration directed phase II study

Abstract Number: 7506
Session Date & Time: Tuesday, June 4, 20199:45 AM – 12:45 PM CT
– Presentation Time: 11:45AM CT
Session Title: Hematologic Malignancies—Lymphoma and Chronic Lymphocytic Leukemia
Location: McCormick Place, Room E451
Lead Author: Nathan Hale Fowler, MD, The University of Texas MD Anderson Cancer Center, Department of Lymphoma/Myeloma
The above abstract is now available via the ASCO (Free ASCO Whitepaper) meeting website at www.asco.org.

Data to be presented at the EHA (Free EHA Whitepaper) meeting:

• Poster Presentation: The novel bispecific CD47-CD19 antibody TG-1801 potentiates the activity of ublituximab-umbralisib (U2) drug combination in preclinical models of B-NHL

Session Date & Time: Saturday, June 15, 2019 17:30 – 19:00 CEST
Session Title: Lymphoma Biology & Translational Research
Location: Amsterdam RAI, Poster Session
Lead Author: Marcelo Lima Ribeiro, Vall d’Hebron University Hospital, Vall d’Hebron Institute of Oncology (VHIO), Autonomous University of Barcelona, Barcelona, Spain
The above abstract will be available today, May 16, 2019 via the EHA (Free EHA Whitepaper) meeting website at www.ehaweb.org.

Data to be presented at the ICML meeting:

• Oral Presentation: A Phase 2 Study to Assess the Safety and Efficacy of Umbralisib in Patients with Chronic Lymphocytic Leukemia (CLL) Who Are Intolerant to Prior BTK or PI3K Delta Inhibitor Therapy

Session Date & Time: Thursday, June 20, 2019 13:45 – 15:15 CEST
– Presentation Time: 15:00 CEST
Session Title: Session 3 – CLL
Location: Palazzo dei Congressi, Room A – Main Hall
Lead Author: Anthony R. Mato, MD, Memorial Sloan Kettering Cancer Center
• Oral Presentation: Phase I/II Study of Umbralisib (TGR-1202) in Combination with Ublituximab (TG-1101) and Pembrolizumab in Patients with Rel/Ref CLL and Richter’s Transformation

Session Date & Time: Thursday, June 20, 2019 17:05 – 18:05 CEST
– Presentation Time: 17:05 CEST
Session Title: Focus on Non-Clinical and Early Clinical Data with New Combinations
Location: Palazzo dei Congressi, Cinema Corso
Lead Author: Anthony R. Mato, MD, Memorial Sloan Kettering Cancer Center
• Oral Presentation: Umbralisib Monotherapy Demonstrates Efficacy and Safety in Patients with Relapsed/Refractory Marginal Zone Lymphoma: A Multicenter, Open-Label, Registration Directed Phase 2 Study

Session Date & Time: Saturday, June 22, 2019 10:15 – 11:15 CEST
– Presentation Time: 10:45 CEST
Session Title: Focus on Indolent Non-Follicular Lymphoma
Location: Palazzo dei Congressi, Room A and B
Lead Author: Pierre-Luigi Zinzani, MD, University of Bologna, Institute of Hematology "L. e A. Seràgnoli"
• Poster Presentation: The novel bispecific CD47-CD19 antibody TG-1801 potentiates the activity of ublituximab-umbralisib (U2) drug combination in preclinical models of B-NHL

Session Date & Time: Wednesday, June 19 (12:00-17:00 CEST), Thursday, 20 (9:00-17:00 CEST) and Friday, June 21 (9:00-18:30 CEST)
Location: Palazzo dei Congressi, Marquee Parco Ciani
Lead Author: Marcelo Lima Ribeiro, Vall d’Hebron University Hospital, Vall d’Hebron Institute of Oncology (VHIO), Autonomous University of Barcelona, Barcelona, Spain
The above abstracts will be available via the ICML meeting website at www.lymphcon.ch on June 12, 2019.

Following each presentation, the data presented will be available on the Publications page, located within the Pipeline section, of the Company’s website at www.tgtherapeutics.com/publications.cfm.

Sutro Biopharma Announces Presentation at the 2019 European Hematology Association Congress

On May 16, 2019 Sutro Biopharma, Inc. (NASDAQ: STRO) reported that the company will present at the upcoming European Hematology Association (EHA) (Free EHA Whitepaper) Congress being held June 13-16, 2019, in Amsterdam (Press release, Sutro Biopharma, MAY 16, 2019, View Source [SID1234536431]). The abstract summarizes preliminary results from the first 14 patients enrolled in the company’s ongoing Phase 1 study of STRO-001, the first antibody-drug conjugate generated with Sutro’s novel cell-free protein synthesis technology, in patients with advanced B-cell malignancies.

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Poster Presentation Details:

Preliminary results of a Phase 1 dose escalation study of the first-in-class anti-CD74 antibody-drug conjugate (ADC), STRO-001, in patients with advanced B-cell malignancies.

Date: Saturday, June 15, 2019

Time: 5:30 p.m. – 7:00 p.m. CEST

Location: Poster Hall, RAI Convention Center, Amsterdam

Poster Session: Aggressive Non-Hodgkin Lymphoma – Clinical

Abstract Number: PS1071

The abstract was published today on the EHA (Free EHA Whitepaper) website. Following the conference, the poster will be accessible through the Clinical/Scientific Presentation and Publication Highlights page of the News section of the company’s website at www.sutrobio.com.