Tolero Pharmaceuticals to Highlight New Data Evaluating Investigational Agents Alvocidib and TP-1287 at 2018 American Society of Hematology Annual Meeting

On November 2, 2018 Tolero Pharmaceuticals, Inc., a clinical-stage company focused on developing novel therapeutics for hematological and oncological diseases, reported that new data from three abstracts on the Company’s pipeline of investigational agents will be presented at the 60th Annual Meeting of the American Society of Hematology (ASH) (Free ASH Whitepaper), December 1-4 in San Diego, California (Press release, Tolero Pharmaceuticals, NOV 2, 2018, View Source [SID1234530690]). Among the presentations, updated data from Zella 201, an ongoing Phase 2 study evaluating the efficacy and safety of alvocidib, a potent CDK9 inhibitor, in combination with cytarabine and mitoxantrone in patients with relapsed or refractory MCL-1-dependent acute myeloid leukemia (AML) will be featured in an oral presentation. Additional data from Tolero’s pipeline will also be presented, including preclinical findings on the activity of alvocidib and decitabine, as well as preclinical data evaluating the activity of TP-1287, an oral CDK9 inhibitor, in combination with bortezomib or venetoclax for the potential treatment of multiple myeloma. Three additional abstracts on Tolero sponsored research will be presented by independent research institutions.

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"We look forward to sharing the latest data from our pipeline at the ASH (Free ASH Whitepaper) Annual Meeting, including updated findings from the Zella 201 study, which further informs our understanding of the potential role of alvocidib in relapsed or refractory MCL-1-dependent acute myeloid leukemia," said David J. Bearss, Ph.D., Chief Executive Officer of Tolero Pharmaceuticals. "These data at ASH (Free ASH Whitepaper) reinforce our commitment and progress in advancing our clinical programs focused on hematologic and oncologic diseases."

Below are the details for the Tolero presentations:

Abstract Title

Details

Presenter

Zella 201: A Biomarker-Guided Phase II
Study of Alvocidib Followed by Cytarabine
and Mitoxantrone in MCL-1 Dependent
Relapsed/ Refractory Acute Myeloid
Leukemia (AML)

Abstract #30

December 1, 8:45 a.m. PT

Oral Presentation

Joshua F. Zeidner,
Lineberger Comprehensive
Cancer Center, University of
North Carolina, Chapel Hill, NC

The Oral CDK9 Inhibitor, TP-1287, Is
Active in Non-Clinical Models of Multiple
Myeloma

Abstract #3269

December 2, 6 – 8 p.m. PT

Poster Presentation

Clifford Whatcott,

Tolero Pharmaceuticals, Inc.

The CDK9 Inhibitor, Alvocidib, Potentiates
the Non-Clinical Activity of Azacytidine or
Decitabine in an MCL-1-Dependent
Fashion, Supporting Clinical Exploration of
a Decitabine and Alvocidib Combination

Abstract #4355

December 3, 6- 8 p.m. PT

Poster Presentation

Wontak Kim, Tolero
Pharmaceuticals, Inc.

Below are selected details for the presentations from Tolero sponsored research:

Abstract Title

Details

The PIM Kinase Inhibitor TP-3654 in Combination with
Ruxolitinib Exhibits Marked Improvement of Myelofibrosis in
Murine Models

Abstract #54

December 1, 8:45 am PT

Oral Presentation

Enhanced Expression of Beta-Catenin and Axl Receptor
Tyrosine Kinase (RTK) in Chronic Lymphocytic Leukemia
(CLL) B-Cells with Co-Culture on Marrow Stromal Cells:
Implications for Leukemic Cell Drug Resistance

Abstract #3125

December 2, 6 – 8 p.m. PT

Poster Presentation

Axl-RTK Inhibition Modulates T Cell Functions and Synergizes
with Chimeric Antigen Receptor T Cell Therapy in B Cell
Malignancies

Abstract #728

December 3, 3 p.m. PT

Oral Presentation

A bout Alvocidib
Alvocidib is an investigational small molecule inhibitor of cyclin-dependent kinase 9 (CDK9) currently being evaluated in a Phase II study, Zella 201, in patients with relapsed or refractory MCL-1 dependent acute myeloid leukemia, AML, in combination with cytarabine and mitoxantrone ( NCT02520011 ). Alvocidib is also being evaluated in Zella 101, a Phase I clinical study evaluating the maximum tolerated dose, safety and clinical activity of alvocidib in combination with (7+3) in newly diagnosed patients with AML ( NCT03298984 ), and Zella 102, a Phase 1b/2 study in patients with myelodysplastic syndromes, MDS, in combination with decitabine ( NCT03593915 ). In addition, alvocidib is being evaluated in a Phase 1 study in patients with relapsed or refractory AML in combination with venetoclax ( NCT03441555 ).

About TP-1287
TP-1287 is an investigational oral cyclin-dependent kinase 9 ( CDK9) inhibitor entering into a Phase 1 study in patients with advanced solid tumors ( NCT03604783) . TP-1287 has shown favorable oral bioavailability in preclinical models. TP-1287 is enzymatically cleaved, yielding the parent drug, alvocidib, a potent inhibitor of CDK9.

About CDK9 Inhibition and MCL-1
MCL-1 is a member of the apoptosis-regulating BCL-2 family of proteins.2 In normal function, it is essential for early embryonic development and for the survival of multiple cell lineages, including lymphocytes and hematopoietic stem cells.3 In MCL-1–dependent AML, MCL-1 inhibits apoptosis and sustains the survival of leukemic blasts, which may lead to relapse or resistance to treatment.2,4 The expression of MCL-1 in leukemic blasts is regulated by cyclin-dependent kinase 9 (CDK9).5,6 Because of the short half-life of MCL-1 (2-4 hours), the effects of targeting upstream pathways are expected to reduce MCL-1 levels rapidly.5 Inhibition of CDK9 has been shown to block MCL-1 transcription, resulting in the rapid downregulation of MCL-1 protein, thus restoring the normal apoptotic regulation.2

FibroGen to Report Third Quarter 2018 Financial Results on Thursday, November 8, 2018

On November 2, 2018 FibroGen, Inc. (NASDAQ: FGEN), a biopharmaceutical company, reported that it will report third quarter 2018 financial results on Thursday, November 8, 2018, after market close, and will host a conference call to discuss financial results and provide a business update at 5:00 p.m. ET (2:00 p.m. PT) (Press release, FibroGen, NOV 2, 2018, View Source;p=irol-newsArticle&ID=2375179 [SID1234530689]).

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Conference Call and Audio Webcast
Interested parties may access a live audio webcast of the conference call via the investor section of the FibroGen website, www.fibrogen.com. It is recommended that listeners access the website 15 minutes prior to the start of the call to download and install any necessary audio software. A replay of the webcast will be available shortly after the call for a period of two weeks. To access the replay, please dial (888) 843-7419 (domestic) or (630) 652-3042 (international), and use passcode 4778 0296#.

Dial-In Information
Live (U.S./Canada): (888) 771-4371
Live (International): (847) 585-4405
Confirmation number: 47780296

Asterias Biotherapeutics to Report Third Quarter 2018 Results on November 12, 2018

On November 2, 2018 Asterias Biotherapeutics, Inc. (NYSE American: AST), a biotechnology company dedicated to developing cell-based therapeutics to treat neurological conditions associated with demyelination and cellular immunotherapies to treat cancer, reported that it will release third quarter 2018 financial and operating results on Monday, November 12, 2018 after the close of the U.S. financial markets (Press release, BioTime, NOV 2, 2018, View Source;p=RssLanding&cat=news&id=2375072 [SID1234530688]). The Company will host a conference call and webcast on November 12, 2018 at 5:00 p.m. ET / 2:00 p.m. PT to discuss the results and corporate developments.

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For both "listen-only" participants and those participants who wish to take part in the question-and-answer portion of the call, the dial-in number in the U.S./Canada is 888-394-8218. For international participants outside the U.S./Canada, the dial-in number is 323-794-2591. For all callers, refer to Conference ID 6651165. To access the live webcast, go to View Source

A replay of the conference call will be available for one month beginning about two hours after the conclusion of the live call, by calling toll-free (from U.S./Canada) 888-203-1112; international callers dial 719-457-0820. Use the Conference ID 6651165. Additionally, the archived webcast will be available at View Source

Sandoz decides not to pursue US biosimilar rituximab; will focus on robust biosimilar portfolio for unmet access and sustainability needs

On November 2, 2018 Sandoz, a Novartis division and the pioneer and global leader in biosimilars, reported that it will not pursue its submission for biosimilar rituximab in the US at this time (Press release, Novartis, NOV 2, 2018, View Source [SID1234530687]). The decision follows a request by the US Food and Drug Administration (FDA) for additional information to complement the submission. Sandoz will focus on progressing its biosimilar pipeline in areas of greatest unmet access needs.

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"We appreciate the important conversations with the FDA, which have provided specific requirements for our potential US biosimilar rituximab, but believe the patient and marketplace needs in the US will be satisfied before we can generate the data required," said Stefan Hendriks, Global Head of Biopharmaceuticals, Sandoz.

"We are disappointed to have to make this decision and stand behind the safety, efficacy and quality of our medicine, which met the stringent criteria for approval in the European Union, Switzerland, Japan, New Zealand and Australia. Given the breadth of our biosimilar pipeline, we believe we should now focus on opportunities in the US and around the world where we can best meet rapidly evolving patient and healthcare system needs."

Sandoz remains committed to enabling early and expanded patient access and creating savings for healthcare systems through a robust biosimilar portfolio. Sandoz has seven approved biosimilars worldwide, three of which are approved in the US, and is currently awaiting marketing authorization in the EU for pegfilgrastim, following a CHMP positive opinion in September 2018.

Novartis data at ASH and SABCS show strength of pipeline and portfolio in hematology and oncology

On November 2, 2018 Novartis reported that it will present new research that may transform the way serious blood diseases and a certain type of breast cancer are treated at the upcoming 60th American Society of Hematology (ASH) (Free ASH Whitepaper) Annual Meeting & Exposition in San Diego, December 1-4 and the 41st Annual San Antonio Breast Cancer Symposium (SABCS), December 4-8 (Press release, Novartis, NOV 2, 2018, View Source [SID1234530686]). Nearly 150 abstracts will be presented across both congresses, underscoring the strength of the Novartis pipeline and portfolio in hematology and oncology.

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"Novartis Oncology has a purpose-driven legacy built on an unwavering commitment to help patients live better and longer lives," said Liz Barrett, CEO, Novartis Oncology. "The breadth and depth of our data at these scientific forums demonstrates how we are acting on our vision to reimagine cancer in a meaningful way for patients by relentlessly pursuing scientific advancements and exploring novel combination treatment options to help those living with hard-to-treat diseases."

Novartis data at the 2018 ASH (Free ASH Whitepaper) Annual Meeting will highlight the following:

Updates on outcomes with Kymriah (tisagenlecleucel) in adult relapsed or refractory (r/r) patients with diffuse large b-cell lymphoma (DLBCL) and pediatric and young adult patients with r/r acute lymphoblastic leukemia (ALL)*:

Updated analysis of the efficacy and safety of tisagenlecleucel in pediatric and young adult patients with relapsed/refractory acute lymphoblastic leukemia [Abstract #895; Monday, December 3, 4:30 PM PT]
Sustained disease control for adult patients with relapsed or refractory diffuse large b-cell lymphoma: an updated analysis of JULIET, a global pivotal Phase 2 trial of tisagenlecleucel [Abstract #1684; Saturday, December 1, 6:15 PM PT]
New post-hoc analysis of the SUSTAIN study evaluating crizanlizumab in patients with sickle cell disease:

Established prevention of vaso-occlusive crises with crizanlizumab is further improved in patients who follow the standard treatment regimen: post-hoc analysis of the Phase II SUSTAIN study [Abstract #1082; Saturday, December 1, 6:15 PM PT]
First reported data for investigational compound asciminib (ABL001) in chronic myeloid leukemia (CML) patients with T315I genetic mutation that causes resistance to most BCR-ABL tyrosine kinase inhibitors (TKIs) approved to treat CML:

Asciminib (ABL001), a specific allosteric BCR-ABL1 inhibitor, in patients with chronic myeloid leukemia and the T315I mutation in a Phase 1 trial [Abstract #792; Monday, December 3, 4:00 PM PT]
New data evaluating dabrafenib and trametinib combination treatment in hairy cell leukemia (HCL):

Treatment with combination of dabrafenib and trametinib in patients with recurrent/refractory BRAF V600E-mutated hairy cell leukemia (HCL) [Abstract #391; Sunday, December 2, 12:00 PM PT]
Data evaluating Promacta/Revolade (eltrombopag) in patients with immune thrombocytopenia (ITP):

Bleeding related episodes, thrombotic events and platelet counts among immune thrombocytopenia patients receiving second line therapy [Abstract #2436; Sunday, December 2, 6:00 PM PT]
Treatment of ITP with eltrombopag in patients who have received prior rituximab: a post hoc analysis of the EXTEND study [Abstract #1152; Saturday, December 1, 6:15 PM PT]
Final results from the ITP World Impact Survey (I-WISh) about the burden of disease and impact of ITP on patient quality of life and productivity:

Patients with immune thrombocytopenia (ITP) frequently experience severe fatigue but it is under-reported by physicians: Results from the ITP World Impact Survey
(I-WISh) [Abstract #2273; Saturday, December 1, 6:15 PM PT]
Patients with immune thrombocytopenia (ITP) experience impaired quality of life (QoL), with negative effects on their daily activities, social interactions, emotional well-being and working lives: Results from the ITP World Impact Survey (I-WISh) [Abstract #4804; Monday, December 3, 6:00 PM PT]
New analyses evaluating Rydapt (midostaurin) in patients with FLT3-mutated acute myeloid leukemia (AML):

Prognostic impact of insertion site in acute myeloid leukemia with FLT3 internal tandem duplication: results from the RATIFY study [Abstract #435; Sunday, December 2, 5:00 PM PT]
RATIFY: prognostic impact of FLT3 tyrosine kinase domain (TKD) and NPM1 mutation status in patients with newly diagnosed acute myeloid leukemia (AML) treated with midostaurin or placebo plus standard chemotherapy [Abstract #2668; Sunday, December 2, 6:00 PM PT]
RADIUS: A phase 2 randomized trial investigating standard of care ± midostaurin after allogeneic stem cell transplant in FLT3-ITD-mutated AML [Abstract #662; Monday, December 3, 10:45 AM PT]
New data evaluating Exjade/Jadenu (deferasirox) in patients with low- and int-1-risk myelodysplastic syndromes (MDS) and chronic iron overload:

Safety and efficacy, including event-free survival, of deferasirox versus placebo in iron-overloaded patients with low- and int-1-risk myelodysplastic syndromes (MDS): outcomes from the randomized, double-blind TELESTO study [Abstract #234; Saturday, December 1, 5:15 PM PT]
New data evaluating Jakavi (ruxolitinib)** for patients with polycythemia vera who are resistant to or intolerant of hydroxyurea:

Long-term efficacy and safety (5 Years) in RESPONSE, a Phase 3 study comparing ruxolitinib (rux) with best available therapy (BAT) in hydroxyurea (HU)-resistant/intolerant patients (pts) with polycythemia vera (PV) [Abstract #1753; Saturday, December 1, 6:15 PM PT]
Additional data presented at ASH (Free ASH Whitepaper) include:

Complete responses in relapsed/refractory acute myeloid leukemia (AML) patients on a weekly dosing schedule of XmAb14045, a CD123 x CD3 T cell-engaging bispecific antibody: initial results of a phase 1 study [Abstract #763; Monday, December 3, 2:45 PM PT]
Sandoz, a Novartis division and the pioneer and global leader in biosimilars will present data for the company’s pegfilgrastim, filgrastim and rituximab biosimilars:

Cost simulation for the US of febrile neutropenia hospitalization due to pegfilgrastim on-body injector failure compared to single-injection pegfilgrastim and daily injections with reference and biosimilar filgrastim in non-Hodgkin lymphoma [Abstract #2251; Saturday, December 1, 6:15 PM PT]
Subcutaneous versus intravenous rituximab in non-Hodgkin lymphoma treated with R-CHOP: economic modeling for the US [Abstract #4776; Monday, December 3, 6:00 PM PT]
Novartis data at the 2018 SABCS Annual Symposium will highlight the following:

New data evaluating Kisqali (ribociclib)*** in broad range of patients with hormone receptor positive, human epidermal growth factor receptor-2 negative (HR+/HER2-) advanced breast cancer:

Biomarker analysis by baseline circulating tumor DNA alterations in the MONALEESA-3 study [Abstract #PD2-05; Wednesday, December 5, 5:00 PM CT]
Ribociclib + endocrine therapy in patients with hormone receptor-positive, HER2-negative advanced breast cancer presenting with visceral metastases: Subgroup analysis of phase III MONALEESA trials [Abstract #P6-18-07; Saturday, December 8, 7:00 AM CT]
Ribociclib with endocrine therapy for premenopausal patients with hormone receptor-positive, HER2-negative advanced breast cancer: Biomarker analyses from the phase III randomized MONALEESA-7 trial [Abstract #PD2-08; Wednesday, December 5, 5:00 PM CT]
Ribociclib treatment benefit in patients with advanced breast cancer with >=1 dose reduction: Data from the MONALEESA-2, -3, and -7 trials [Abstract #P6-18-06; Saturday, December 8, 7:00 AM CT]
Additional updates on investigational treatments, BYL719 (alpelisib) and LSZ102:

Alpelisib + fulvestrant for advanced breast cancer: Subgroup analyses from the Phase III SOLAR-1 trial [Abstract #GS3-08; Thursday, December 6, 11:15 AM CT]
Phase 1/1b study of novel oral selective estrogen receptor degrader (SERD) LSZ102 for estrogen receptor-positive (ER+) advanced breast cancer (ABC) with progression on endocrine therapy (ET) [Abstract #PD1-08; Wednesday, December 5, 5:00 PM CT]
Sandoz will present US real-world evidence data surrounding cost-effectiveness through use of the company’s biosimilar filgrastim-sndz:

Potential Medicare beneficiary out-of-pocket cost reductions through use of biosimilar filgrastim-sndz over reference filgrastim among breast cancer patients: a simulation model analysis [Abstract #675; Friday, December 7, 5:00 PM CT]
Throughout the 2018 ASH (Free ASH Whitepaper) Annual Meeting and SABCS Annual Symposium, Novartis will host dedicated content on View Source that will feature unique insights and perspectives on emerging areas of cancer care and research.

Product Information
Approved indications for products vary by country and not all indications are available in every country. The product safety and efficacy profiles have not yet been established outside the approved indications. Because of the uncertainty of clinical trials, there is no guarantee that compounds will become commercially available with additional indications.

For full prescribing information, including approved indications and important safety information about marketed products, please visit View Source

Asciminib (ABL001), crizanlizumab (SEG101), alpelisib (BYL719) and LSZ102 are investigational compounds. Efficacy and safety have not been established. There is no guarantee these compounds will become commercially available.