SOTIO has stopped collaboration trial with the dendritic cell vaccine DCVAC in combination with ONCOS-102

On February 9, 2021 Targovax ASA (OSE: TRVX), a clinical stage immuno-oncology company developing immune activators to target hard-to-treat solid tumors, reported that collaboration partner SOTIO has stopped the combination trial assessing the combination of ONCOS-102 and DCVAC/PCa in prostate cancer (Press release, Targovax, FEB 9, 2021, View Source [SID1234574767]). Only a very limited patient population fulfilled the strict inclusion criteria. Therefore, the recruitment could not meet originally planned numbers.

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The phase I trial prostate cancer study was paid for and run by the Czech biotech company SOTIO, investigating whether ONCOS-102 could enhance the efficacy of SOTIO´s dendritic cell vaccine DCVAC/PCa. Targovax has generated promising data in melanoma and mesothelioma, and the decision will not impact the further development of ONCOS-102.

Patient recruitment has been slow due to limited patient population availability. In combination with additional COVID-19 related challenges, SOTIO has decided to stop the trial after four patients enrolled. This was a phase I safety trial, and an analysis of clinical outcomes will be submitted at a future scientific conference.

CStone Announces Another Breakthrough Therapy Designation Granted for Sugemalimab, Representing a New Breakthrough in the Treatment of Relapsed and Refractory Lymphoma

On February 8th, 2021 CStone Pharmaceuticals, a leading biopharmaceutical company focused on developing and commercializing innovative immuno-oncology therapies and precision medicines, reported that anti-PD-L1 antibody sugemalimab has been granted Breakthrough Therapy Designation (BTD) by the China National Medical Products Administration (NMPA) Center for Drug Evaluation (CDE) for the treatment of patients with relapsed or refractory extranodal natural killer/T-cell lymphoma (R/R ENKTL) (Press release, CStone Pharmaceauticals, FEB 8, 2021, View Source [SID1234633505]). In addition to this major milestone, sugemalimab was granted Orphan Drug Designation (ODD) for the treatment of T-cell lymphoma and BTD for the treatment of R/R ENKTL by the U.S. Food and Drug Administration (FDA) in October 2020.

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The NMPA’s BTD is designed to facilitate the development and expedite the review of novel medicines to treat serious conditions and fulfill an unmet medical need, specifically for novel or "me-better" candidates at the clinical stage, which has demonstrated significant clinical advantages over the available treatment options. The BTD approval from the China NMPA is expected to substantially accelerate the development and commercialization of sugemalimab in China.

The BTD is supported by the promising CS1001-201 Phase II results in patients with R/R ENKTL, which were presented at the annual meeting of the Chinese Society of Clinical Oncology (CSCO) in 2020. Among 38 evaluable patients, the objective response rate (ORR) was 44.7%, the complete response (CR) rate was 31.6%, and the median duration of response (mDoR) was 16.8 months. Of all 43 patients who received sugemalimab, the median overall survival (mOS) was 19.7 months, and the one-year OS rate was 55.5%. Additionally, sugemalimab demonstrated favorable safety and tolerability.

Professor Huiqiang Huang of Sun Yat-sen University Cancer Center, the Principal Investigator of CS1001-201 study said, "R/R ENKTL is a highly malignant and aggressive disease, in addition to the lack of efficacious treatment options, which often leads to poor prognosis, low cure rate, and severe unmet medical needs of patients. The preliminary results have indicated that sugemalimab could potentially become a new treatment option for patients with R/R ENKTL."

Dr. Jason Yang, Chief Medical Officer of CStone, commented, "We are excited that sugemalimab has been granted BTD by the China NMPA, which also makes sugemalimab one of the very few domestic novel drugs that have obtained BTD from the Agencies in both the U.S. and China. This designation underscores the remarkable clinical value of sugemalimab, and we look forward to working closely with the NMPA in China to maximize the benefit of sugemalimab to patients in the nearest future."

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About ENKTL

Extranodal natural killer/T-cell lymphoma (ENKTL) is a subtype of mature T cell and NK cell lymphoma. There is no existing effective salvage treatment for patients with R/R ENKTL who failed L-asparaginase-based standard regimen. Patients also respond poorly to conventional treatments. Clinicians often have limited treatment options for such patients due to rapid disease progression and poor survival outcomes with a one-year survival rate of less than 20%. In China, the currently available targeted monotherapy for these patients has a complete response (CR) rate of approximately 6%. Thus, there are significant unmet medical needs in patient who failed first-line treatment.

About CS1001-201 Study

CS1001-201 is a single-arm, multicenter, Phase II pivotal study designed to evaluate the efficacy and safety of sugemalimab as monotherapy for the treatment of adult patients with R/R ENKTL. The primary endpoint of this study is ORR as assessed by the Independent Radiology Review Committee (IRRC). On August 14th, 2020, CS1001-201 has received a Study May Proceed (SMP) letter from the U.S. FDA for the Investigational New Drug (IND) application. CS1001-201 was currently ongoing in the U.S. and China.

About Sugemalimab

Sugemalimab is an investigational anti-PD-L1 monoclonal antibody discovered by CStone. Authorized by the U.S.-based Ligand Corporation, sugemalimab is developed by the OmniRat transgenic animal platform, which can generate fully human antibodies in one stop. As a fully human, full-length anti-PD-L1 monoclonal antibody, sugemalimab mirrors the natural G-type immunoglobulin 4 (IgG4) human antibody, which reduce the risk of immunogenicity and potential toxicities in patients, a unique advantage over similar drugs.

Sugemalimab has completed a Phase 1 dose-escalation study in China. During Phase 1a and Phase 1b of the study, sugemalimab showed good antitumor activity and tolerability in multiple tumor types.

Currently, sugemalimab is being investigated in a number of ongoing clinical trials. In addition to a Phase 1 bridging study in the U.S., the clinical program in China includes one multi-arm Phase 1b study for several tumor types, one Phase 2 registration studies for lymphoma, and four Phase 3 registration studies, respectively, for stage III/IV NSCLC, gastric cancer, and esophageal cancer. The phase 3 trial of sugemalimab in the treatment of stage IV non-small cell lung cancer reached the primary endpoint. The U.S. Food and Drug Administration has granted Breakthrough Therapy Designation to anti-PD-L1 antibody sugemalimab for the treatment of adult patients with relapsed or refractory extranodal natural killer/T-cell lymphoma in October 2020. The China National Medical Products Administration has accepted the company’s New Drug Application for sugemalimab.

Cue Biopharma Initiates Patient Dosing in Phase 1 Study of CUE-101 in Combination with KEYTRUDA® (pembrolizumab) as First-line Treatment for HPV+ Recurrent/Metastatic Head and Neck Cancer

On February 8, 2021 Cue Biopharma, Inc. (Nasdaq: CUE), a clinical-stage biopharmaceutical company engineering a novel class of injectable biologics designed to selectively engage and modulate targeted T cells within the patient’s body, reported that on February 1, 2021, the first patient was dosed in a Phase 1 dose escalation clinical trial of CUE-101 in combination with Merck’s anti-PD-1 therapy, KEYTRUDA (pembrolizumab) (Press release, Cue Biopharma, FEB 8, 2021, View Source [SID1234608286]). CUE-101 is being evaluated in combination with KEYTRUDA as first-line treatment for human papilloma virus positive recurrent/metastatic head and neck squamous cell carcinoma (HPV+ R/M HNSCC).

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"We are very pleased to have initiated our combination trial of CUE-101 with KEYTRUDA," said Ken Pienta, M.D, acting chief medical officer of Cue Biopharma. "In our ongoing dose escalation monotherapy Phase 1 trial, CUE-101 has been well tolerated at doses where we’ve observed preliminary evidence of clinical activity, and in preclinical studies we’ve demonstrated that the combination of CUE-101 and checkpoint blockade appear synergistic by significantly extending survival in mouse models of HPV positive cancers. These data taken together support our belief that the combination of CUE-101 with KEYTRUDA has the potential to enhance anti-tumor activity and prolong patient survival."

This Phase 1 dose escalation combination trial (NCT03978689) is being conducted in parallel at the same clinics that are conducting the ongoing Phase 1 monotherapy study of CUE-101. Due to the tolerability profile demonstrated to date in the CUE-101 monotherapy dose escalation trial, the first dose in the combination arm is 1 mg/kg every three weeks (Q3W), which is also the recommended dosing interval for KEYTRUDA.

KEYTRUDA is a registered trademark of Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc., Kenilworth, NJ, USA.

About the CUE-100 Series
The CUE-100 series consists of Fc-fusion biologics that incorporate peptide-MHC (pMHC) molecules along with rationally engineered IL-2 molecules. This singular biologic is anticipated to selectively target, activate and expand a robust repertoire of tumor-specific T cells directly in the patient. The binding affinity of IL-2 for its receptor has been deliberately attenuated to achieve preferential selective activation of tumor-specific effector T cells while reducing potential for effects on regulatory T cells (Tregs) or broad systemic activation, potentially mitigating the dose-limiting toxicities associated with current IL-2-based therapies.

About Immuno-STAT
The company’s Immuno-STAT (Selective Targeting and Alteration of T cells) biologics are designed for targeted modulation of disease-associated T cells in the areas of immuno-oncology and autoimmune disease. Each of our biologic drugs is designed using our proprietary scaffold comprising: 1) a pMHC to provide selectivity through interaction with the T cell receptor (TCR), and 2) a unique co-stimulatory signaling molecule to modulate the activity of the target T cells.

The simultaneous engagement of co-regulatory molecules and pMHC binding mimics the signals delivered by antigen presenting cells (APCs) to T cells during a natural immune response. This design enables Immuno-STAT biologics to engage with the T cell population of interest, resulting in highly targeted T cell modulation. Because our drug candidates are delivered directly in the patient’s body (in vivo), they are fundamentally different from other T cell therapeutic approaches that require the patients’ T cells to be extracted, modified outside the body (ex vivo), and reinfused.

Press Release: Onco-immunology Company Pan Cancer T Launched as Spin-off from Erasmus Medical Center

On February 8, 2021 Pan Cancer T B.V., a biotech spin-off from the Erasmus MC founded by Prof. Dr. Reno Debets (CSO) and Dr. Dora Hammerl (VP R&D), reported the closing of a seed investment and start of operations (Press release, Pan Cancer T, FEB 8, 2021, https://pancancer-t.com/2021/02/07/life-saving-tcr-t-cell-therapies-for-hard-to-treat-solid-tumors/ [SID1234577957]). Together with Katrien Reynders-Frederix (CEO), the team is committed to the discovery and development of novel TCR therapies against solid tumors such as triple negative breast cancer, bladder cancer, lung cancer, and glioma. Seed investors are Swanbridge Capital and Van Herk Ventures, and the young company is further awarded a Health~Holland grant for a public-private-partnership with Erasmus MC.

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Over the past decades, innovations in cancer treatments have improved the survival of cancer patients. Despite successes of therapies like Chimeric Antigen Receptor (CAR) T-cell therapies, the vast majority of solid cancers remain refractory to such treatments. Pan Cancer T introduces new treatment options for hard-to-treat solid cancers through adoptive therapy with T-cells that are genetically engineered with TCRs. TCR therapy exploits the ability of the immune cells, in this case T-cells, to specifically and efficiently recognize and kill malignant cells according to the expression of intracellular target antigens. The company develops safe and first-in-class TCR T-cell therapies against unique and proprietary targets that are exclusively expressed in multiple tumor types, but absent in healthy tissues. In addition, the company delivers smart treatments that act against tumor micro-environmental hurdles and maximizes the efficacy of TCR T-cells towards solid tumors.

Katrien Reynders-Frederix, CEO of Pan Cancer T, said: "Immunotherapy currently holds a large potential for cancer treatment. Adoptive T-cell therapy is one of the most promising approaches that has already proven its feasibility and clinical benefit in tumors in several clinical trials. The team is committed to develop safe and potent therapies, and the first data underscore the potential of our lead program where T-cells are directed against the PCT-1 target. Thanks to the support of our investors and Health~Holland, we are able to advance our pre-clinical programs. I am honored to be part of a company that has the potential to positively impact millions of lives. We are looking forward to further expanding our investor base and raising a Series A financing round to accelerate our programs."

Reno Debets, CSO of Pan Cancer T, Professor at Erasmus MC and specialist in T-cell immunity and adoptive therapy of tumors, stated: "The fact that tumors grow and metastasize is often a consequence of immune evasion, pointing to the inherent ability of T-cells to selectively recognize and potently destruct tumors. To translate this ability towards patient care, we exploit fundamental platforms established over the last decade in our laboratory. Our platforms cover tumor-selective targets for T-cells; technologies to identify safe and effective TCRs; as well as strategies to overcome T-cell suppressive effects of the tumor micro-environment. It is exactly this research fundament that goes head-on against the current challenges of immunotherapies. I am really proud and confident that with our enthusiastic team we will make important steps towards improved patient care".

Thijs Spigt, Director of Technology Transfer Office at Erasmus MC Rotterdam: "Erasmus MC’s mission is to provide excellence in patient care, education and research. A key strategic element supporting this mission is the valorization of research findings. The establishment of Pan Cancer T, together with Swanbridge and Van Herk, fits a series of perfect examples how Erasmus MC is able to translate excellent research into development of new therapies for difficult to treat cancer types. We continue to support the team, and look forward to a prosperous future for the company".

Cillian King, Investment Manager at Swanbrigde Capital, commented: "Recent advances in our understanding of the immune system and its role in cancer have resulted in the uptake of many new immunotherapies into clinical practice. However, despite remarkable results for some patients, many patients still lack effective treatment options, particularly those with solid tumors with immune suppressive microenvironments. We believe the science, expertise, and vision behind Pan Cancer T has the potential to profoundly impact patient outcomes and we look forward to supporting the company along this exciting journey".

Herantis Pharma to Participate in the Upcoming Swiss Nordic Bio Conference

On February 8, 2021 Herantis Pharma Plc ("Herantis"), an innovative clinical stage biotech company pioneering new disease modifying and regenerative biologic and gene therapies, reported that Craig Cook, Chief Executive Officer, will hold a company presentation in the upcoming Swiss Nordic Bio Conference investor conference, this year taking place virtually (Press release, Herantis Pharma, FEB 8, 2021, View Source,c3282325 [SID1234577479]).

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Event Details:

Swiss Nordic Bio Conference

10 – 11 February 2021

On 11 February 2021 all presentations will be available via a digital library, which is accessible to event participants only. Please contact the organizers at the Swiss Nordic Bio Conference if you wish to attend.