Moderna to Provide Business and Pipeline Updates at the 2019 J.P. Morgan Healthcare Conference

On January 2, 2019 Moderna, Inc. (Nasdaq: MRNA), a clinical stage biotechnology company pioneering messenger RNA (mRNA) therapeutics and vaccines to create a new generation of transformative medicines for patients, reported that CEO Stéphane Bancel will present an update on the Company and its pipeline of mRNA development programs at this year’s 37th annual J.P. Morgan Healthcare Conference (Press release, Moderna Therapeutics, JAN 2, 2019, View Source [SID1234532368]).

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Mr. Bancel’s presentation will take place on Tuesday, January 8, 2019 at 10:30 a.m. PT in the Colonial Room at The Westin St. Francis Hotel in San Francisco. The presentation will be followed by a question and answer session. A live webcast of both the presentation and question and answer session can be accessed on the investors section of Moderna’s website at investors.modernatx.com. A replay of the webcast also will be archived on Moderna’s website for up to 30 days following the presentation.

Atreca to Present at the 37th Annual J.P. Morgan Healthcare Conference

On January 2, 2018 Atreca, Inc., a biotechnology company focused on developing novel therapeutics based on a deep understanding of the human immune response, reported that John A. Orwin, President and Chief Executive Officer, will present at the 37th Annual J.P. Morgan Healthcare Conference on Tuesday, January 8, 2019, at 1:30 p.m. Pacific Standard Time in San Francisco, CA (Press release, Atreca, JAN 2, 2019, View Source [SID1234532367]).

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Clovis Oncology to Present at the 37th Annual J.P. Morgan Healthcare Conference

On January 2, 2019 Clovis Oncology, Inc. (Nasdaq: CLVS) reported that its Chief Executive Officer and President, Patrick J. Mahaffy, will present at the 37th Annual J.P. Morgan Healthcare Conference on Tuesday, January 8, 2019 at 4:30 p.m. Pacific time (Press release, Clovis Oncology, JAN 2, 2019, View Source [SID1234532366]). The conference will be held at the Westin St. Francis Hotel in San Francisco.

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A live webcast of the presentation and Q&A session can be accessed through the investor relations section of the Company’s website at www.clovisoncology.com. Following the live presentation, a replay of the webcast will be available on the Company’s website for 30 days.

Forbius to Present at the 37th Annual J.P. Morgan Healthcare Conference

On January 2, 2019 Forbius, a clinical-stage company developing biologics for the treatment of fibrosis and cancer, reported that Ilia Tikhomirov, CEO of Forbius, will be presenting at the 37th Annual J.P. Morgan Healthcare Conference (Press release, Forbius, JAN 2, 2019, View Source [SID1234532365]).

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Mr. Tikhomirov’s presentation will take place Wednesday, January 9th at 11:30 am PST in Elizabethan D at the Westin St. Francis Hotel in San Francisco.

First-in-human Study of Precision Immune Stimulant PIN-2 Demonstrated Pharmacologic Activity and Safety in Patients with Advanced Solid Tumors

On January 2, 2019 PIN Pharma, Inc., reported final results of a first-in-human clinical trial of its novel immunomodulating agent PIN-2 in subjects with advanced solid tumors (Press release, PIN Pharma, JAN 2, 2019, View Source [SID1234532363]).

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This was an open-label, repeat-dose study with a primary objective to assess the pharmacodynamic activity of PIN-2. Pharmacodynamic biomarkers that signal changes in the human immune system were used to assess the immunomodulatory potential of PIN-2. Biomarkers evaluated as part of the primary end point were the following: tumor necrosis factor alpha (TNF-α), interferon gamma (IFN-γ), and interleukin-12 (IL-12). The secondary end points were the following: characterization of the safety profile of PIN-2, its plasma pharmacokinetics, and its immunogenicity.

The study, conducted in Australia by PIN Pharma’s wholly owned Australian subsidiary, PIN Pharma Pty Ltd, included 8 patients who received a dose of 300 µg of PIN-2 intravenously, 3 times per week for 2 weeks, followed by a 1-week rest period. A second cycle of treatment was offered according to patient and investigator preference.

There was a rapid onset of action as evidenced by a marked increase in circulating TNF-α 6 hours post PIN-2 injection, which returned to baseline. A similar but more pronounced finding was observed during a second cycle of treatment. This finding demonstrated proof-of-mechanism for the immunomodulatory effect of PIN-2 and corroborated results observed in human monocytes in vitro. No clear changes were observed in the other biomarkers.

PIN-2 was generally safe and well tolerated, with grade 2 infusion-related reactions seen in 3 patients, who responded promptly to standard therapy. The drug was rapidly cleared from plasma. Anti-drug antibodies that did not impact the pharmacodynamic end point developed in 2 patients.

Colin Bier, PhD, CEO, said, "We are pleased that, in patients with advanced malignancy who failed to respond to multiple therapeutic regimens, PIN-2 demonstrated a signal indicating induction of innate immune activation as evidenced by the rapid rise in TNF-α, which is a key early mediator of the immune response. This is a result we predicted on the basis of previously reported transcriptomic studies. These study findings clearly support additional clinical trials to assess the clinical efficacy and safety profile of our novel immunomodulating agent. We plan to present complete results of the trial at an oncology congress in 2019."

About PIN-2

PIN-2 is a novel immunomodulatory peptide with a unique mechanism of action in that it links the innate and adaptive immune systems, resulting in an enhanced immune response. In vitro and in vivo preclinical studies have shown that PIN-2 rapidly and preferentially penetrates monocytes, modifies the mRNAs involved in the induction of innate immune activation (with an attendant link to the adaptive immune system), and promotes endogenous cytotoxic T lymphocytes infiltration at the tumor site. PIN-2 acts upstream of other immune-based treatment modalities.

In a validated, highly aggressive breast cancer mouse model, PIN-2 was shown to impact tumor progression and increase survival (in combination with cyclophosphamide), override tumor-mediated immune resistance, and reduce distant site metastasis (in combination with a checkpoint inhibitor.)

Given its unique, upstream immunomodulatory activity, its extensive preclinical body of evidence, and its first-in-human study results, PIN-2 holds the potential to be a new strategy in the fight against cancer and cancer-mediated immunosuppression. Further clinical research is warranted to evaluate the full potential of PIN-2 in cancer care.