Karyopharm to Report Fourth Quarter and Full Year 2019 Financial Results on February 13, 2020

On February 6, 2020 Karyopharm Therapeutics Inc. (Nasdaq:KPTI), an oncology-focused pharmaceutical company, reported that it will report fourth quarter and full year 2019 financial results on Thursday, February 13, 2020 (Press release, Karyopharm, FEB 6, 2020, View Source [SID1234553946]). Karyopharm’s management team will host a conference call and audio webcast at 8:30 a.m. ET on Thursday, February 13, 2020, to discuss the financial results and other company updates.

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To access the conference call, please dial (855) 437-4406 (local) or (484) 756-4292 (international) at least 10 minutes prior to the start time and refer to conference ID 4367549. A live audio webcast of the call will be available under "Events & Presentations" in the Investor section of the Company’s website, View Source An archived webcast will be available on the Company’s website approximately two hours after the event.

Jounce Therapeutics Presents New Vopratelimab Predictive Biomarker Data Supporting Use in the Upcoming SELECT Trial at the 2020 ASCO-SITC Clinical Immuno-Oncology Symposium Annual Meeting and Announces Research Collaboration with NanoString Technologies

On February 6, 2020 Jounce Therapeutics, Inc. (NASDAQ: JNCE), a clinical-stage company focused on the discovery and development of novel cancer immunotherapies and predictive biomarkers, reported new data on the identification of the predictive biomarker to be used for patient selection in the SELECT clinical trial of vopratelimab (vopra), in addition to a research collaboration with NanoString (NASDAQ: NSTG) (Press release, Jounce Therapeutics, FEB 6, 2020, View Source [SID1234553945]). The new data introduces TISvopra, a baseline RNA signature with a threshold optimized for the emergence of ICOS hi CD4 T cells, a vopratelimab pharmacodynamic biomarker not associated with PD-1 inhibitor therapy. When applied to ICONIC clinical data, TISvopra predicted clinical outcomes from the ICONIC trial better than PD-L1 immunohistochemistry (IHC). These results are being presented today at the 2020 ASCO (Free ASCO Whitepaper)-SITC Clinical Immuno-Oncology Symposium Annual Meeting in Orlando, Florida.

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"We are excited to announce these two new developments supporting our upcoming SELECT clinical trial of vopratelimab and our own PD-1 inhibitor. The new data presented today at ASCO (Free ASCO Whitepaper)-SITC reveal the identification of TISvopra as a baseline predictive biomarker associated with the emergence of ICOS hi CD4 T cells. When applied to ICONIC clinical data, TISvopra then predicted clinical benefit in patients who received vopratelimab alone or in combination with nivolumab. This, coupled with our new research collaboration with NanoString, reflects our commitment to patient selection strategies to identify those most likely to benefit from our novel immunotherapies," said Elizabeth Trehu, M.D., chief medical officer of Jounce Therapeutics. "The identification of TISvopra is a crucial step forward in the development of vopratelimab, and we plan to initiate the Phase 2 SELECT trial using this biomarker in mid-2020."

Key highlights from the poster, titled "Association of a Predictive RNA Signature (RS) With Emergence of ICOS hi CD4 T Cells and Efficacy Outcomes for the ICOS Agonist Vopratelimab (vopra) and Nivolumab (nivo) in Patients (pts) on the ICONIC trial" include:

TISvopra is an 18 gene RNA Tumor Inflammation Signature (TIS), utilized with a vopratelimab-specific threshold and was identified as a biomarker predictive of ICOS hi CD4 T cell emergence. TISvopra positive patients treated with vopratelimab alone or in combination with nivolumab also showed improved clinical benefit (response rate, six month and nine month landmark progressive free survival and overall survival) as compared with TISvopra negative patients in the ICONIC trial.
TIS includes genes associated with integral elements of CD4 T cell activation that may contribute to a more comprehensive immune response.
The TISvopra threshold was chosen to optimize prediction of ICOS hi CD4 T cell emergence and was more predictive of clinical benefit than PD-L1 IHC in the ICONIC trial.
The emergence of ICOS hi CD4 T cells is a vopratelimab, but not a PD-1 inhibitor, pharmacodynamic biomarker linked to clinical benefit in the ICONIC trial.
In the upcoming SELECT trial, TISvopra will be used to select patients for treatment with vopratelimab and JTX-4014, Jounce’s PD-1 inhibitor.
The poster is available in the "Our Pipeline" section of the Jounce Therapeutics website under "Publications" at www.jouncetx.com.

Jounce also announced a research collaboration with NanoString to support the application of the predictive biomarker to be used in the SELECT trial. Under the terms of the collaboration, Jounce and NanoString will apply an optimized selection threshold of the TIS based on the emergence of ICOS hi CD4 T cells (TISvopra). The TISvopra clinical trial assay will be implemented on the nCounter Dx Analysis System.

About the Phase 2 SELECT Clinical Trial
The Phase 2 SELECT clinical trial is a randomized, ex-U.S. trial to evaluate the efficacy of JTX-4014 alone and in combination with vopratelimab. The trial is powered to show statistical superiority of vopratelimab plus JTX-4014 compared to JTX-4014 alone in a biomarker-selected patient population. Jounce expects to enroll approximately 75 immunotherapy naïve second-line non-small cell lung cancer (NSCLC) patients. Patients will be prescreened for the TISvopra biomarker. Jounce estimates that approximately 20% of the prescreened NSCLC patients will be above the TISvopra threshold and potentially eligible for the trial. Jounce expects to initiate the SELECT trial in mid-2020 and report preliminary efficacy and biomarker relationships to clinical outcomes from up to 75 patients in 2021.

About Vopratelimab
Jounce’s lead product candidate, vopratelimab, is a clinical-stage monoclonal antibody that binds to and activates ICOS, the Inducible T cell CO-Stimulator, a protein on the surface of certain T cells commonly found in many solid tumors. Vopratelimab is currently being assessed in the Phase 2 EMERGE clinical trial in a sequenced combination with ipilimumab in patients with NSCLC who were previously treated with PD-1/PD-L1 inhibitor therapies. Jounce is also planning to initiate the Phase 2 SELECT clinical trial of vopratelimab with its investigational PD-1 inhibitor, JTX-4014, in TISvopra biomarker-selected patients. Vopratelimab was previously assessed in the Phase 1/2 ICONIC trial and was found to be safe and well-tolerated, alone and in combination with each of the anti-PD-1 antibodies nivolumab and pembrolizumab, as well as with ipilimumab, an antibody that binds to CTLA-4.

IGM Biosciences to Present at Two Upcoming Investor Conferences

On February 6, 2020 IGM Biosciences, Inc. (Nasdaq: IGMS), a global leader in the research and development of engineered therapeutic IgM antibodies, reported that Fred Schwarzer, Chief Executive Officer, will present at two upcoming investor conferences (Press release, IGM Biosciences, FEB 6, 2020, View Source [SID1234553944]):

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Guggenheim Healthcare Talks Idea Forum Oncology Day on Thursday, February 13 at 1:30 p.m. ET in New York.
Cowen and Company 40th Annual Health Care Conference on Monday, March 2 at 2:10 p.m. ET in Boston.
A live webcast of the events will be available on the "Events and Presentations" page in the "Investors" section of the Company’s website at View Source A replay of the webcasts will be archived on the Company’s website for 90 days following the presentation.

Genprex to Focus on Developing Immunogene Therapy, Start Lung Cancer Trials This Year

On February 5, 2020 Genprex reported that after receiving the US Food and Drug Administration’s fast track designation last month for its immunogene therapy Oncoprex in combination with the EGFR tyrosine kinase inhibitor (TKI) osimertinib (AstraZeneca’s Tagrisso), the clinical-stage gene therapy company is prioritizing development of this therapy combination for EGFR-mutated non-small cell lung cancer and will start enrollment in Phase I/II clinical trials in mid-2020 (Press release, Genprex, FEB 5, 2020, View Source [SID1234553943]).

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Enrollment will start after the FDA accepts Genprex’s amendment to its investigational new drug application.

The company also said last month that it intends to start a new Phase I clinical trial investigating Oncoprex in combination with a checkpoint inhibitor. This is supported by preclinical studies indicating that TUSC2 increases the effectiveness of anti-PD1 checkpoint blockade combined with chemotherapy for lung metastases with KRAS and LKB1 mutations in mice.

Oncoprex is Genprex’s lead product candidate and it uses the active agent TUSC2 (Tumor Suppressor Candidate 2) gene combined with a lipid nanovesicle. TUSC2 has been shown to disrupt replication and proliferation of cancer cells, re-establish programmed cell death, as well as modulate the immune response against cancer cells. It’s also been observed to block mechanisms that create drug resistance.

Additionally, the company is putting its current Phase I/II trial investigating Oncoprex in combination with EGFR inhibitor erlotinib (Genentech/Roche’s Tarceva) ─ which provided support for the fast track designation ─ on hold, citing the reason that osimertinib is now considered the new standard of care of NSCLC patients with an EGFR mutation. Genprex has treated more than 50 lung cancer patients with Oncoprex in Phase I/II trials.

Purdue-discovered ‘fluorescent markers’ to illuminate cancer, improve outcomes, receives FDA fast track as Phase 3 clinical trials begin

On February 6, 2020 On Target Laboratories Inc., a privately held biotechnology company developing the use of Purdue University-discovered fluorescent markers to target and illuminate cancer during surgery, reported that it has announced the results of a multi-institutional Phase 2 clinical trial in which outcomes were improved for 26% of patients undergoing pulmonary resection for non-small-cell lung cancer (NSCLC) (Press release, On Target Laboratories, FEB 6, 2020, View Source,-improve-outcomes,-receives-fda-fast-track-as-phase-3-clinical-trials-begin.html [SID1234553942]).

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The results of the treatment, called OTL38, were presented at the 56th annual Meeting of the Society of Thoracic Surgeons (STS), held last month in New Orleans, and were featured in a plenary session as a J. Maxwell Chamberlain Memorial Paper for General Thoracic Surgery, considered to be among the top-rated abstracts at STS. The treatment was developed in the Purdue laboratory of Philip Low in the Purdue Institute of Drug Discovery. Low is the Presidential Scholar for Drug Discovery and Ralph C. Corley Distinguished Professor of Chemistry-Biochemistry in the Department of Chemistry. Currently, there are 288 clinical trials performed or in process using Purdue-developed medical treatments at 4,841 sites across the globe.

"Our goal is to provide surgeons with new technology to help them provide a more complete resection to more patients. This gives patients the best chance of improved outcomes after surgery," said Christopher Barys, president and CEO of On Target Laboratories.

Lung cancer is the leading cause of cancer-related deaths in the United States. Pulmonary resection, either a wedge resection, segmentectomy, or lobectomy, is recommended for most patients who have operable stage I-II non-small cell lung cancer. Intraoperative molecular imaging (IMI) — also referred to as fluorescence-guided surgery — may increase the likelihood of a more complete surgical resection, which could translate into increased survival for patients and reduced re-operations or adjuvant treatment for hospitals.

Conducted over 18 months, the study included 92 patients eligible for analysis. There were no drug-related serious adverse events and 24 patients, or 26%, were impacted during pulmonary resection, with 8% of patients having a change in their stage due to the use of IMI.

The study showed that IMI improved localization of small and peripheral lesions, which can be difficult for surgeons to identify visually or through manual palpitation, and enabled localization of otherwise unlocalizable lesions in 11 patients, or 12%. Further, 10 additional cancers were found in seven patients, or 8%. During the Specimen Check Phase, when the surgeon confirms that the nodule is in the specimen and analyzes the margins, surgeons thought all margins were adequate, yet back-table inspection using IMI revealed inadequate margins in eight patients, or 9%.

"OTL38 is the first technique that is specific to imaging adenocarcinomas of the lung, which is one of the most common types of invasive lung cancer," said Dr. Inderpal (Netu) S. Sarkaria of the Department of Cardiothoracic Surgery at the University of Pittsburgh Medical Center. "Near-infrared imaging with OTL38 may be a powerful tool to help surgeons significantly improve the quality of lung cancer surgery by more clearly identifying tumors and allowing the surgeon to better see and completely remove them — one of the most vital components in the overall care of patients with this disease."

OTL38 is under development in two Phase 3 clinical trials for lung and ovarian cancer indications. Both trials are being conducted under a special protocol agreement with the U.S. Food and Drug Administration. OTL38 also has received a fast-track designation for both the lung and ovarian cancer indications and an orphan designation for ovarian cancer from the FDA.

Low is a co-founder of On Target and the technology is licensed through the Purdue Research Foundation Office of Technology of Commercialization. The Purdue Institute of Drug Discovery is situated near Discovery Park District, a $1 billion-plus long-term enterprise to support a transformational center of innovation on the western edge of the Purdue University campus. The district includes the Convergence Center for Innovation and Collaboration, where startups, entrepreneurs, innovators and companies can collaborate with Purdue to address global challenges in health, sustainability, IT and space. The district already includes a public airport with a 7,000-foot runway, and partnerships with international companies including Rolls-Royce, Schweitzer Engineering Laboratories and Saab. Visit Discovery Park District.

About Intraoperative Molecular Imaging

To date, there have been limited ways for surgeons to confidently assess the location and full extent of cancerous tissue while operating. On Target Laboratories’ fluorescent markers are composed of a near-infrared dye and a targeting molecule, or ligand, that binds to receptors overexpressed on cancer cells. These markers illuminate the cancerous lesions, lighting the way for the resection of malignant tissue and enabling surgeons to see and remove more diseased tissue. On Target’s first novel compound, OTL38, targets folate receptors commonly found on many cancers, including lung and ovarian cancers. A small single dose of the compound is administered via IV infusion one to 24 hours before surgery, allowing the surgeon to identify malignant tissue during the procedure using the near-infrared camera.