HTG Technology Featured Across Numerous Abstracts at Upcoming Scientific Conferences
Several of the company’s key biopharma customers and scientific collaborators from
There will be at least three poster presentations at SABCS 2022, being held in
- PD-17-05 – Development and Validation of a Composite Biomarker Predictive of Palbociclib + Endocrine Treatment Benefit in Early Breast Cancer: PENELOPE-B and PALLAS Trials. First author Dr.
Sibylle Loibl fromGBG Forschungs GmbH - PD17-06 – Immunohistochemical Markers and Determinants of Clinical Response in the Penelope-B Trial. First author Dr.
Erik Knudsen fromRoswell Park Comprehensive Cancer Center - P3-05-09 – vLAG3+ Tumor Infiltrating Lymphocytes Predict Outcome in Treatment Naïve Triple Negative Breast Carcinoma. First author Dr.
Shikha Bose fromCedars Sinai Medical Center
During the ASH Meeting, which will take place in
- 1529 – Biomarker Analysis of Zanubrutinib and Tislelizumab Combination Therapy in Patients with Relapsed/Refractory B-Cell Malignancies. Presented by Jiaoyan Lyu from BeiGene
- 2874 – Deep Peripheral T Cell Immune-Profiling in Relapsed/Refractory Non-Hodgkin Lymphoma: Evaluation of Baseline Samples from the Epcoritamab Epcore NHL-1 Trial. Presented by Dr.
Jordan Blum from Genmab - 2859 – Transcriptomic Comparison of Non-Hodgkin Lymphomas in Relapsed/Refractory Versus Newly Diagnosed Patients Using Single FFPE Slides. Presented by Dr.
Omar Jabado from Genmab - 4144 – Bone Marrow Fibrosis Is Associated with Non-Response to CD19 CAR-T Therapy. Presented by
Joshua Anil fromPerelman School of Medicine - 4265 – Durable Responses from Acalabrutinib in Combination with Rituximab, Cyclophosphamide, Doxorubicin, Vincristine and Prednisolone (R-CHOP) As First Line Therapy for Patients with Diffuse Large B-Cell Lymphoma (DLBCL): The Accept Phase Ib/II Single Arm Study. Presented by Dr.
Andrew J. Davies from Southampton Cancer ResearchUK Centre.
“The abstracts being presented at these conferences reflect the important research being conducted by our customers and collaborators,” said
About HTG:
HTG is accelerating precision medicine from diagnosis to treatment by harnessing the power of transcriptome-wide profiling to drive translational research, novel therapeutics and clinical diagnostics across a variety of disease areas.
Building on more than a decade of pioneering innovation and partnerships with biopharma leaders and major academic institutes, HTG’s proprietary RNA platform technologies are designed to make the development of life science tools and diagnostics more effective and efficient and to unlock a differentiated and disruptive approach to transformative drug discovery. For more information visit www.htgmolecular.com.
Forward-Looking Statements:
Statements contained in this press release regarding matters that are not historical facts are “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995, including statements regarding the capabilities and benefits of HTP, the design and benefits of HTG’s RNA platform technologies, and other statements related to the future. Words such as “designed to,” “believe,” “anticipate,” “expect,” “potential,” “will” and similar expressions are intended to identify forward-looking statements, although not all forward-looking statements necessarily contain these identifying words. These forward-looking statements are based upon management’s current expectations, are subject to known and unknown risks, and involve assumptions that may never materialize or may prove to be incorrect. Actual results and the timing of events could differ materially from those anticipated in such forward-looking statements as a result of various risks and uncertainties, including, without limitation, risks associated with drug discovery and development; the risk that HTP and our RNA platform and medicinal chemistry technologies may not provide the benefits that we expect\the risk that our products and services may not be adopted by biopharmaceutical companies or other customers as anticipated, or at all; our ability to manufacture our products to meet demand; competition in our industry; additional capital and credit availability; our ability to attract and retain qualified personnel; risks associated with the impact of the COVID-19 pandemic on us and our customers; and product liability claims. These and other factors are described in greater detail in our filings with the Securities and Exchange Commission (SEC), including under the “Risk Factors” heading of our Quarterly Report on Form 10-Q for the quarter ended September 30, 2022, as filed with the SEC on November 10, 2022. All forward-looking statements contained in this press release speak only as of the date on which they were made, and we undertake no obligation to update such statements to reflect events that occur or circumstances that exist after the date on which they were made.
HTG Investor Contact:
Ashley Robinson
Phone: (617) 430-7577
Email: arr@lifesciadvisors.com

Source: HTG Molecular Diagnostics, Inc.