Idera Pharmaceuticals Shares Positive Results from Investigator-Sponsored Trial in Melanoma Patients at Amsterdam UMC

On May 17, 2022 Idera Pharmaceuticals, Inc. ("Idera," "we," and "our") (Nasdaq: IDRA) reported that positive interim results from Amsterdam UMC, Vrije Universiteit Amsterdam, the Netherlands, regarding its investigator-sponsored trial, INTRIM 1, involving tilsotolimod, Idera’s synthetic Toll-like receptor 9 agonist. Based on these results, the trial has been stopped early (Press release, Idera Pharmaceuticals, MAY 17, 2022, View Source [SID1234614737]).

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INTRIM 1 is a randomized, double-blind, placebo-controlled Phase 2 trial among patients with localized, excised melanoma (pathological tumor stage 3-4) with no regional metastases detected and no evidence of distant metastasis. The trial involved a single, intradermal injection of 8 mg tilsotolimod or saline placebo given at the primary tumor excision site, followed by re-excision and sentinel lymph node (SLN) biopsy 7-10 days later. Noting that there were more patients with ulcerated lesions in the placebo arm compared to the tilsotolimod arm, topline interim results of the respective SLN-positivity rates showed a 70% lower SLN+ rate among patients injected with tilsotolimod as compared to those injected with placebo; the placebo SLN+ rate was in the mid-40%s. Statistical significance exceeded the pre-specified p-value of 0.008. Adverse reactions included injection site reactions, malaise, fever and flu-like symptoms.

"This is an exciting result from tilsotolimod, and we are pleased for the patients and their families to whom it offers hope for the future," said Vincent Milano, Idera’s Chief Executive Officer. "These results, together with data supporting tilsotolimod’s mechanism of action and encouraging safety profile from across the array of earlier pre-clinical and clinical work, reinforce the potential of tilsotolimod to offer benefit to patients with certain cancers. As a result, we plan to actively pursue a strategic partnership for tilsotolimod so that its full potential for patients may continue to be explored."

This interim result validates previously reported results from INTRIM 1 that showed immune activation, including elevated frequencies of key dendritic cells, in early analysis by flow cytometry of the SLN biopsies. The trial will continue to relapse-free survival (RFS) and overall survival (OS) at 5 and 10 years after SLN biopsy.

"Currently, there are limited adjuvant treatments available to improve survival after surgical excision of a primary melanoma," said Prof. Tanja de Gruijl of Amsterdam UMC. "We are delighted with the results we have seen in this study, which suggest that tilsotolimod administered at the excision site lowers the extent of tumor-positive lymph nodes and, if it improves overall survival, offers early melanoma patients a potential new treatment option." Amsterdam UMC investigators plan to present the full data set at an upcoming medical meeting.

About Melanoma

Melanoma is a cancer that begins in a type of skin cell called melanocytes. While melanoma is the least common type of skin cancer, it has a poor prognosis when not detected and treated early. Early stages of melanoma are treated by removing, or excising, the tumor surgically. However, even after surgery, nearly one-third of all melanoma patients will experience disease recurrence and most relapses eventually will progress to metastatic disease. When regional lymphatic metastases are present, the 10-year survival rate is 68% – 24%. SLN biopsy is a useful prognostic tool for the assessment of melanoma relapse and mortality risk. Ulceration is associated with more SLN positivity.

In many cases, additional cancer treatment, referred to as adjuvant therapy, is given after the primary excision of the melanoma. The goal of adjuvant therapy is to reduce the risk of melanoma returning and potentially metastasizing. The adjuvant market size for melanoma excision cases is over 1 million cases globally and about 300,000 in the US annually. As is the case in many forms of cancer, melanoma becomes more difficult to treat once the disease has spread, or metastasized, beyond the skin to other parts of the body.

About INTRIM 1

INTRIM 1 is a multi-center investigator-sponsored trial conducted by UMC Amsterdam among patients with pT3-4 cN0M0 melanoma. The study is a randomized, double-blind, placebo-controlled Phase 2 trial of a single, intradermal injection of 8 mg tilsotolimod or of saline placebo given at the primary tumor excision site 7-10 days prior to SLN biopsy.

INTRIM 1 is intended to examine the ability of tilsotolimod to induce loco-regional and systemic immune stimulation, and therefore, improve survival among the targeted patient population. Outcome measures of the trial include the following:

· Primary endpoint: rate of tumor positive SLN at the time of biopsy.
·Secondary endpoints:
·Immune response in the SLN and peripheral blood 7-10 days post-biopsy, as measured by frequency and activation state of lymph node resident (LNR) conventional dendritic cells (DC) and melanoma antigen-specific T cell responses in the SLN and peripheral blood.
·RFS, determined by the length of time from intradermal injection of tilsotolimod to first documentation of recurrence (RFS), measured at 5 and 10 years after SLN biopsy.
·OS at 5 and 10 years after SLN biopsy, determined by the length of time from intradermal injection of tilsotolimod to death from any cause.

While enrollment for the primary endpoint has been halted early as a result of the primary endpoint being met, the study will continue to its secondary endpoints. For more information on the INTRIM 1 trial, please visit www.ClinicalTrials.gov (NCT04126876).

About Tilsotolimod (IMO-2125)

Tilsotolimod is an investigational, synthetic Toll-like receptor 9 agonist. Tilsotolimod has been shown to promote both innate (Type-I IFN, antigen presentation) and adaptive (T cells) immune activation and may, in turn, contribute to tumor suppression and regression. For more information on tilsotolimod trials, please visit www.ClinicalTrials.gov.

New Guidelines from AUA and ASTRO Support Inclusion of Genomic Testing in Localized Prostate Cancer

On May 17, 2022 Myriad Genetics reported that According to the American Cancer Society, in 2022 more than 268,000 men in the United States will be diagnosed with prostate cancer, making it the second most common cancer in men (Press release, Myriad Genetics, MAY 17, 2022, View Source [SID1234614908]). Tragically, close to 35,000 men will die from prostate cancer in 2022. About 1 in 8 men will be diagnosed with prostate cancer during his lifetime.

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Last week, we attended the 2022 American Urological Association (AUA) National Meeting. It was an informative three days spent exploring the latest advancements in urology and showcasing the power of genetic insights to personalize prostate cancer treatment.

While at the meeting, AUA and American Society for Radiation Oncologists (ASTRO) shared updated guidelines that support including genomic testing in localized prostate cancer.

For the first time, prognostic biomarker tests, such as Myriad Genetics’ Prolaris Prostate Cancer Test, are specifically cited in the guidelines as a potential tool that can be used to incorporate personalized genomic insights into prostate cancer care and clinical treatment decision-making. Additionally, the guidelines recommend physicians perform a risk assessment to help guide the decision to offer germline testing, including an analysis of mutations associated with aggressive prostate cancer or are known to have implications for treatment.  

The inclusion of tumor prognostic and germline testing represents another step forward to offer a clearer and more personalized treatment path for men with prostate cancer.

Genetic insights for more actionable and personalized prostate cancer treatment

Myriad Genetics is the only lab offering the combination of both prognostic tumor analysis and germline testing for individuals affected by prostate cancer.

 Prolaris is a prognostic, tumor-based mRNA expression test that measures the aggressiveness of a man’s prostate cancer. It combines a genomic tumor aggressiveness score with traditional, diagnostic features like Prostate-Specific Antigen (PSA), Gleason, and tumor stage, helping physicians identify which patients are safe for active surveillance, would benefit from a single mode of therapy, or require greater intensity of treatment.  Prolaris has already been broadly recommended by the National Comprehensive Cancer Network (NCCN) for use in low, intermediate and high-risk disease.

Myriad offers germline testing with its MyRisk Hereditary Cancer Test, as well as its FDA-approved companion diagnostic test, BRACAnalysis CDx, which helps identify patients that are most likely to benefit from PARP-inhibitor therapy based on germline BRCA1/BRCA2 status.

More than three million patients have been tested to date with our MyRisk, Prolaris, and companion diagnostic tests.  Prognostic tests, like Prolaris, and germline companion diagnostic tests, like BRACAnalysis CDx, can help better determine the behavior of a patient’s tumor, providing actionable data-driven information physicians need to create an individualized treatment plan.

For more information on how Myriad Genetics continues to innovate and improve the health and well-being for men with prostate cancer. Click here: View Source

Protara Therapeutics to Present at the H.C. Wainwright Global Investment Conference

On May 17, 2022 Protara Therapeutics, Inc. (Nasdaq: TARA), a clinical-stage company developing transformative therapies for the treatment of cancer and rare diseases, reported that management will present at the H.C. Wainwright Global Investment Conference being held May 23 through May 26, 2022 (Press release, Protara Therapeutics, MAY 17, 2022, View Source [SID1234614723]).

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The prerecorded presentation will become available on Tuesday, May 24, 2022 at 7:00 a.m. ET and can be accessed by visiting the Events and Presentations section of the Company’s website: View Source The webcast will be archived for 90 days following the presentation.

MacroGenics to Participate in Upcoming Investor Conference

On May 17, 2022 MacroGenics, Inc. (Nasdaq: MGNX), a biopharmaceutical company focused on developing and commercializing innovative antibody-based therapeutics for the treatment of cancer, reported that the Company’s management will participate in the following investor conference in May 2022 (Press release, MacroGenics, MAY 17, 2022, View Source [SID1234614740]).

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H.C. Wainwright Global Investment Conference. MacroGenics’ President & Chief Executive Officer, Scott Koenig, M.D., Ph.D., will provide a corporate overview in Miami, FL, on Wednesday, May 25, 2022, at 11:30 am ET. Management will also participate in one-on-one meetings.
A webcast of the above presentation may be accessed under "Events & Presentations" in the Investor Relations section of MacroGenics’ website at View Source The Company will maintain an archived replay of this webcast on its website for 30 days.

Transgene Announces Upcoming Investor Meetings

On May 17, 2022 Transgene (Euronext Paris: TNG) (Paris:TNG), a biotech company that designs and develops virus-based immunotherapeutics against cancer, reported that Management will participate in the upcoming investor events set out below (Press release, Transgene, MAY 17, 2022, View Source [SID1234614757]):

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– UBS Global Healthcare Conference
May 23-25, 2022
New York City, NY, USA

– Spring European MidCap Event
June 23-24, 2022
Paris, France

– Conference Portzamparc
June 29, 2022
Paris, France