Dynavax Announces Data Presentations at AACR Annual Meeting

On March 17, 2016 Dynavax Technologies Corporation (NASDAQ: DVAX) reported that it will present data at the American Association for Cancer Research (AACR) (Free AACR Whitepaper) Annual Meeting next month in New Orleans, Louisiana (Press release, Dynavax Technologies, MAR 17, 2016, View Source [SID:1234509605]). The details for the poster presentations are as follows:

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Date and Time: Monday, April 18, 2016, 1:00 p.m. – 5:00 p.m. EDT

Abstract Title: SD-101, a novel intratumoral class C CpG-ODN, given with low-dose radiation in patients with untreated low-grade B-cell lymphoma: interim results of a phase I trial

Session Title: Phase I Clinical Trials 1

Abstract Control Number: 7361

Permanent Abstract Number: CT047

Location: Convention Center, Halls G-J, Poster Section 13

Poster Board Number: 3

Please click here for the full abstract. The poster presentation with updated data will be made available on or after April 18, 2016.

Date and Time: Monday, April 18, 2016, 1:00 p.m. – 5:00 p.m. EDT

Abstract Title: Intratumoral treatment with a highly interferogenic TLR9 agonist reverts tumor escape from PD-1 blockade

Session Title: Immune Checkpoints 1

Abstract Control Number: 4045

Permanent Abstract Number: 2322

Location: Convention Center, Halls G-J, Poster Section 26

Please click here for the full abstract. The poster presentation with updated data will be made available on or after April 18, 2016.

Date and Time: Wednesday April 20, 2016, 8:00 a.m. – 12:00 p.m. EDT

Abstract Title: Radiation potentiates systemic anti-tumor immunity unleashed by a novel TLR9 agonist (SD-101)

Session Title: Immune Modulation from Non-Immunotherapy and Antibodies: Clinical

Abstract Number: 4985

Location: Convention Center, Halls G-J, Poster Section 26

Poster Board Number: 9

Please click here for the full abstract. The poster presentation with updated data will be made available on or after April 20, 2016.

About SD-101

SD-101, the subject of AACR (Free AACR Whitepaper) abstracts CT047, 2322 and 4985, is Dynavax’s proprietary, second-generation, CpG-C class oligodeoxynucleotide TLR 9 agonist. SD-101 activates multiple anti-tumor mechanisms of innate immune cells and activates plasmacytoid dendritic cells to stimulate T cells specific for antigens released from dying tumor cells. TLR9 agonists such as SD-101 enhance T and B cell responses and induce high levels of Type I interferons and maturation of plasmacytoid dendritic cells and B cells. SD-101 is being evaluated in several Phase 1/2 oncology studies to assess its preliminary safety and activity.

OncoSec Announces Presentation at Upcoming American Association for Cancer Research (AACR) Annual Meeting 2016

On March 17, 2016 OncoSec Medical Incorporated ("OncoSec") (NASDAQ: ONCS), a company developing DNA-based intratumoral cancer immunotherapies, reported that new clinical data will be presented at the upcoming American Association of Cancer Research (AACR) (Free AACR Whitepaper) Annual Meeting to be held on April 16-20, 2016 in New Orleans, LA (Press release, OncoSec Medical, MAR 17, 2016, View Source [SID:1234509604]).

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This new data relates to the Company’s Phase II monotherapy clinical study of its investigational intratumoral plasmid IL-12 with electroporation (IT-pIL12-EP) in patients with melanoma. After completing treatment with IT-pIL12-EP, a subset of patients subsequently received anti-PD-1/PD-L1 therapies. Patients with documented follow-up history and evaluable for anti-PD-1/PD-L1 response were included in this single-site retrospective analysis.

Details of the presentation are as follows:

Abstract Title: Intratumoral electroporation of plasmid IL-12 can prime response to anti-PD1/PD-L1 blockade in patients with Stage III/IV-M1a melanoma (Abstract #CT134)
Session Title: Early Clinical Trials Evaluating Cell-based Checkpoint Inhibitors and Novel Immunotherapeutics
Date and Time: April 19, 2016 at 3:45 – 4:00 PM
Location: Room 343, Morial Convention Center

AACR 2016: Innate Pharma displays broad innovative pipeline in immuno-oncology

On March 17, 2016 Innate Pharma SA (the "Company" – Euronext Paris: FR0010331421 – IPH) reported that new preclinical data will be presented at the American Association Of Cancer Research (AACR) (Free AACR Whitepaper) Annual Meeting 2016 taking place from 16 to 20 April 2016, in New Orleans, Louisiana, USA (Press release, Innate Pharma, MAR 17, 2016, View Source [SID:1234509600]).

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These data supports the rationale of four of Innate’s clinical and preclinical programs:

One poster will present preclinical data supporting the rationale for combining an NKG2A checkpoint inhibitor with a PD-1 or a PD-L1 checkpoint inhibitor in mouse models;
One poster will present new data reinforcing the rationale for IPH4301, a first-in-class anti-MICA/B humanized antibody;
Three posters will present preclinical data on new discovery programs targeting CD73 and CD39, immune checkpoints regulating the adenosine pathway, including one poster reporting data generated by OREGA Biotech, Innate’s collaborator on the CD39 project.
Nicolai Wagtmann, Chief Scientific Officer of Innate Pharma, said: "The AACR (Free AACR Whitepaper) annual meeting is one of the major events in our field. This year, we are proud to present 5 posters, demonstrating the progress of our pipeline and the excellence of Innate Pharma’s science. These data supports the rationale and the potential of our assets, and strengthens Innate’s unique positioning in the immuno-oncology field".

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Beyond posters presentations, Innate Pharma’s team will be present with a booth (#2604) to receive its peers and the financial community at AACR (Free AACR Whitepaper).

Nicolai Wagtmann, Chief Scientific Officer of Innate Pharma, will hold a conference call to the attention of analysts and portfolio managers to discuss the data published and Company’s innovative pipeline.

Time and dial in: Tuesday, April 19th 10:30am Eastern Time

USA: 888 504 7963

International: +1 719 325 2452

Access code: 1890466

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About the posters to be presented at the AACR (Free AACR Whitepaper) Annual Meeting 2016:

IPH4301, an antibody targeting MICA and MICB exhibits potent cytotoxic activity and immunomodulatory properties for the treatment of cancer

Permanent Abstract Number: 1491
Session Category: Immunology
Session Title: Immune Modulating Agents and Therapeutic Antibodies
Session Date and Time: Monday Apr 18, 2016 8:00 AM – 12:00 PM
Location: Convention Center, Halls G-J, Poster Section 25
Presented by Mathieu Bléry, PhD
NKG2A immune checkpoint blockade enhances the anti-tumor efficacy of PD1/PD-L1 inhibitors in a preclinical model

Permanent Abstract Number: 2342
Session Category: Immunology
Session Title: Immune Checkpoints 1
Session Date and Time: Monday Apr 18, 2016 1:00 PM – 5:00 PM
Location: Convention Center, Halls G-J, Poster Section 26
Presented by Pascale André, PhD
Discovery and characterization of new original blocking antibodies targeting the CD73 immune checkpoint for cancer immunotherapy

Permanent Abstract Number: 2344
Session Category: Immunology
Session Title: Immune Checkpoints 1
Session Date and Time: Monday Apr 18, 2016 1:00 PM – 5:00 PM
Location: Convention Center, Halls G-J, Poster Section 26
Presented by Ivan Perrot, PhD
Disruption of the CD39 immune checkpoint pathway increases the efficacy of various anticancer therapies in syngeneic mouse models

Permanent Abstract Number: 3218
Session Category: Immunology
Session Title: Immune Checkpoints 2
Session Date and Time: Tuesday Apr 19, 2016 8:00 AM – 12:00 PM
Location: Convention Center, Halls G-J, Poster Section 25
Presented by Jérémy Bastid, PharmD, PhD (OREGA Biotech)
Preclinical development of a humanized blocking antibody targeting the CD39 immune checkpoint for cancer immunotherapy

Permanent Abstract Number: 3222
Session Category: Immunology
Session Title: Immune Checkpoints 2
Session Date and Time: Tuesday Apr 19, 2016 8:00 AM – 12:00 PM
Location: Convention Center, Halls G-J, Poster Section 25
Presented by Ivan Perrot, PhD

Halozyme To Present Data From Five Preclinical Studies At American Association Of Cancer Research Annual Conference

On March 17, 2016 Halozyme Therapeutics (NASDAQ: HALO), a biotechnology company developing novel oncology and drug-delivery therapies,reported that it will present preclinical data from five studies at the American Association of Cancer Research (AACR) (Free AACR Whitepaper) annual conference next month, including results from its ongoing research of lead investigational agent, PEGPH20, and two novel pipeline assets engineered for increased action in the tumor microenvironment (Press release, Halozyme, MAR 17, 2016, View Source [SID:1234509599]). The AACR (Free AACR Whitepaper) annual conference will take place April 17-20 in New Orleans.

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The new Halozyme research builds on previously published data demonstrating increased concentration of immune cells, immunotherapies and chemotherapies in animal models when delivered in combination with PEGPH20. The studies that will be presented at AACR (Free AACR Whitepaper) show enhanced efficacy of checkpoint inhibitors on tumor growth inhibition when treated with PEGPH20, further expanding the company’s growing body of preclinical research supporting PEGPH20’s mechanism of action and potential applicability across multiple types of cancer therapy.

In addition, Halozyme will share data from two novel Halozyme-developed pipeline assets, an immune checkpoint inhibitor that targets adenosine in the tumor microenvironment and an anti-EGFR antibody-drug conjugate.

"We are pleased to share the research of our talented scientists to build on our study of novel agents targeting the tumor microenvironment," said Dr. Helen Torley, president and chief executive officer. "This new work continues to demonstrate the potential ability of PEGPH20 to increase tumor growth inhibition and the accumulation of co-administered therapies across a range of tumor types. We are also excited to share the first details of two pipeline assets that we believe hold great promise for the future."

Dr. Torley and Halozyme Chief Scientific Officer, Dr. Michael LaBarre will host a meeting for investment professionals during the AACR (Free AACR Whitepaper) conference to review data included in the abstracts. The meeting will take place on Monday, April 18 at 4 p.m. ET (3 p.m. CT, 1 p.m. PT). The event will be webcast live through the "Investors" section of Halozyme’s corporate website and a recording will be made available following the close of the event.

To access the webcast and additional documents related to the event, please visit www.halozyme.com approximately fifteen minutes prior to the start time to register, download and install any necessary audio software. The live event may be accessed by calling (877) 410-5657 (domestic callers) or (334) 323-7224 (international callers) using passcode 987221. A telephone replay will be available after the event by dialing (877) 919-4059 (domestic callers) or (334) 323-0140 (international callers) using replay passcode 13259083.

Halozyme’s AACR (Free AACR Whitepaper) abstracts include:

PEGylated recombinant hyaluronidase PH20 enhances pemetrexed antitumor efficacy in a human non-small cell lung cancer model, Sun., April 17, 1-5 p.m. CT
Preclinical evaluation of a next-generation EGFR targeting antibody-drug conjugate that promotes regression in KRAS and BRAF tumors, Mon., April 18, 8 a.m. – noon CT
Enzymatic depletion of adenosine by PEGylated, engineered adenosine deaminase 2 (PEG-ADA2): a novel immunotherapeutic approach to treat solid tumors, Mon., April 18, 8 a.m. – noon CT
PEGPH20 increases the anticancer activity of standard chemotherapy combinations, vincristine (VIN) and D actinomycin (DACT), in a Wilms xenograft model, Mon., April 18, 1-5 p.m. CT
PEGylated recombinant hyaluronidase PH20 (PEGPH20) enhances checkpoint inhibitor efficacy in syngeneic mouse models of cancer, Weds., April 20, 8 a.m. – noon CT
About PEGPH20
PEGPH20 is an investigational PEGylated form of Halozyme’s proprietary recombinant human hyaluronidase under clinical development for the potential systemic treatment of tumors that accumulate hyaluronan. FDA granted orphan drug designation to PEGPH20 for treatment of pancreatic cancer and fast track for PEGPH20 in combination with gemcitabine and nab-paclitaxel for the treatment of metastatic pancreatic cancer.

Additionally, the European Commission, acting on the recommendation from the Committee for Orphan Medicinal Products of the European Medicines Agency, designated investigational drug PEGPH20 an orphan medicinal product for the treatment of pancreatic cancer.

Epizyme to Present New Data in Support of Tazemetostat Clinical Development Program

On March 17, 2016 Epizyme, Inc. (NASDAQ:EPZM), a clinical stage biopharmaceutical company creating novel epigenetic therapies for cancer patients, reported that data from five accepted abstracts of tazemetostat (EPZ-6438), its clinical stage inhibitor of EZH2, will be presented during the American Association for Cancer Research (AACR) (Free AACR Whitepaper) Annual Meeting 2016 being held April 16-20 in New Orleans (Press release, Epizyme, MAR 17, 2016, View Source [SID:1234509613]).

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Tazemetostat is a first-in-class EZH2 inhibitor currently in phase 2 studies in advanced B-cell non-Hodgkin lymphoma (NHL) and certain genetically defined solid tumors. Among the data to be presented at the meeting are studies on the food effect and drug interaction characteristics of tazemetostat.

"We are pleased to be able to present these important new data, including mechanism of action and biomarker studies that continue to guide us in developing patient selection criteria for tazemetostat," said Peter Ho, M.D., Ph.D., Chief Medical Officer, Epizyme. "Additionally, the clinical pharmacology studies being presented have helped to more fully inform the dosing of patients in our ongoing clinical programs."

Planned Presentations:

Evidence of EZH2 Dependent and Independent Mechanisms of Tazemetostat Treatment Emergent Resistance in Models of Diffuse Large B Cell Lymphoma

Speaker: Carly T. Campbell, Epizyme, Inc.
Session Title: Mechanisms of Drug Resistance 1
Abstract Number: 312
Poster Number: 23
Presentation Time: Sunday, April 17, 2016, 1:00 PM – 5:00 PM

Development and Application of a 62-gene Panel for Assessment of Somatic Sequence and Structural Variants in Tumor DNA Derived from non-Hodgkin Lymphoma Patients Treated in a Phase 1 Clinical Trial with the EZH2 Inhibitor Tazemetostat

Speaker: Scott R. Daigle, Epizyme, Inc.
Session Title: Genomic Profiling of Cancers
Abstract Number: 137
Poster Number: 21
Presentation Time: Sunday, April 17, 2016, 1:00 PM – 5:00 PM

The Effect of Tazemetostat on CYP3A-mediated Metabolism of Midazolam in Patients with Solid Tumors

Speaker: Sherri Smith
Session Title: Phase I Clinical Trials in Progress
Abstract Number: CT029
Poster Number: 10
Presentation Time: Monday April 18, 2016 8:00 AM – 12:00 PM

The Effect of Food on the Pharmacokinetics of Tazemetostat in patients with Cancer

Speaker: Benjamin Suttle
Session Title: Phase I Clinical Trials in Progress
Abstract Number: CT031
Poster Number: 12
Presentation Time: Monday April 18, 2016 8:00 AM – 12:00 PM

The Effect of EPZ011989, an Enhancer of Zeste Homolog 2 Inhibitor, in Acute Myeloid Leukemia

Speaker: Sydney Fobare, Hendrix College, Conway, AR
Session Title: Histone Modifications and Chromatin Dynamics
Abstract Number: 4520
Poster Number: 7
Presentation Time: Wednesday, April 20, 8:00 AM – 12:00 PM

About EZH2 in Cancer

EZH2 is a histone methyltransferase (HMT) that is increasingly understood to play a potentially oncogenic role in a number of cancers. These include non-Hodgkin lymphoma, INI1-negative cancers such as malignant rhabdoid tumors and epithelioid sarcomas, certain SMARCA4-negative solid tumors, synovial sarcoma, and a range of other solid tumors.

About Tazemetostat

Epizyme is developing tazemetostat for the treatment of patients with non-Hodgkin lymphoma and for patients with certain genetically defined solid tumors. Tazemetostat is a first-in-class small molecule inhibitor of EZH2 created by Epizyme using its proprietary product platform. In some human cancers, aberrant EZH2 enzyme activity results in dysregulation of genes that control cell proliferation resulting in the rapid and unconstrained growth of tumor cells. Tazemetostat is the WHO International Non- Proprietary Name (INN) for compound EPZ-6438.

Additional information about tazemetostat, including clinical trial information, can be found here.