(Filing, 10-Q, TNI BioTech, MAY 15, 2013, View Source [SID:1234502812])

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Announcing the Acquisition of Exclusive Distribution Rights to Cynviloq™ for the European Union

On May 13, 2013 Sorrento Therapeutics reported the acquisition of exclusive distribution rights from Samyang Biopharmaceuticals to Cynviloq (marketed as Genexol-PM in South Korea) in the 27 countries of European Union (EU) (Press release Sorrento Therapeutics, MAY 13, 2013, View Source [SID:1234500326]). IGDRASOL had previously obtained the exclusive U.S. distribution rights to Cynviloq from Samyang. STI has the right to acquire IGDRASOL pursuant to a previously-announced option agreement, entered into in March 2013.

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Lilly Announces Enzastaurin Phase III Study Did Not Meet Primary Endpoint in Diffuse Large B-Cell Lymphoma

On May 10, 2013 Eli Lilly reported Phase III clinical trial results from enzastaurin’s PRELUDE study, which explored the molecule as a monotherapy in the prevention of relapse in patients with diffuse large B-cell lymphoma (DLBCL) (Press release Eli Lilly, MAY 10, 2013, View Source [SID:1234501030]). The study failed to show a statistically significant increase compared to placebo in disease-free survival in patients at high risk of relapse following rituximab-based chemotherapy. There were no new safety findings, and the safety data were consistent with previously disclosed studies.

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"We are disappointed in the results that we’re announcing today," said Richard Gaynor, M.D., vice president, product development and medical affairs for Lilly Oncology. "However, our oncology pipeline is still one of the most robust across the industry containing more than 20 molecules, including two Phase III molecules in five different tumor types."

Lilly plans to present data from this study at an upcoming scientific meeting.

Lilly will stop development of enzastaurin, which is expected to result in a second-quarter charge to R&D expense of approximately $30 million. The company’s previously-issued financial guidance for 2013 remains unchanged.

About the Study
Patients enrolled in PRELUDE had histologically confirmed DLBCL with an International Prognostic Index (IPI) score of three to five at diagnosis. The IPI is a simple, clinical tool that is used to predict survival outcomes for patients with DLBCL. Patients enrolled also achieved a complete response or complete response-unconfirmed to cyclophosphamide, doxorubicin, vincristine, and prednisone, plus rituximab (R-CHOP) therapy. Patients were randomized in a 2:1 fashion to receive enzastaurin or placebo.

Treatment continued until patients developed progression of disease, unacceptable adverse events, or completed three years of therapy.

Safety and Pharmacokinetics of ALRN-5281, a Long-Acting Growth-Hormone-Releasing-Hormone Agonist, Established in Single-Ascending Dose Study

On May 7, 2013 Aileron Therapeutics, Inc. reported the completion of the first-in-human study of its lead Stapled Peptide drug, ALRN-5281, a proprietary, long-acting growth-hormone-releasing hormone (GHRH) agonist for treating orphan endocrine disorders, including adult growth hormone (GH) deficiency and human immunodeficiency virus (HIV) lipodystrophy, as well as broader patient populations involving a wide variety of metabolic/endocrine diseases (Press release, Aileron Therapeutics, MAY 7, 2013, View Source [SID1234522290]).

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"We are proud to pioneer the first clinical trial of Stapled Peptides, and we look forward to continuing our leadership in the development and eventual commercialization of this promising therapeutic class."

"The successful translation of a Stapled Peptide drug into human subjects has long been our goal. It is an important milestone for Aileron, as well as for the rapidly emerging Stapled Peptide field as a whole," said Joseph A. Yanchik, III, president, chief executive officer and co-founder of Aileron. "We are proud to pioneer the first clinical trial of Stapled Peptides, and we look forward to continuing our leadership in the development and eventual commercialization of this promising therapeutic class."

The initial Phase 1 trial evaluated the safety and tolerability of single ascending doses of ALRN-5281 administered by subcutaneous injection in healthy adult subjects. Additional study objectives included the evaluation of pharmacokinetics (PK) and exploratory pharmacodynamic (PD) biomarkers of ALRN-5281. Thirty-two subjects completed the study. There were no serious adverse events, dose-limiting safety findings, or tolerability issues leading to withdrawal during the study.

"We now have clinical data showing that Aileron’s Stapled Peptides are capable of delivering a drug product profile previously believed to be out of reach with traditional peptide-based therapeutics, in particular PK attributes that support once-weekly dosing," said Hubert C. Chen, M.D., vice president of clinical development at Aileron. "We are encouraged by the prospects of ALRN-5281 to demonstrate improved safety, efficacy, and convenience over currently available GH and GHRH injections. The results of this initial trial will guide us in optimizing dose selection and frequency for ALRN-5281 as a potential best-in-class therapy."

Stapled Peptides are a new class of drugs with a unique set of properties that fully capitalize on 25 years of genetic research to attack drivers of complex diseases, including cancer, endocrine/metabolic disorders and inflammation. The Stapled Peptide platform locks peptides into their biologically active shape and imparts pharmaceutical stability within the body. Stapled Peptide drugs, such as ALRN-5281, are derived from natural peptides and are designed to remain in a safe and effective therapeutic range longer than traditional peptide hormones. This new class of drugs represents a fundamental scientific breakthrough as they offer the most advanced way to replicate normal human physiology to treat human disease.

About ALRN-5281

ALRN-5281 is a proprietary, long-acting GHRH agonist for treating orphan endocrine disorders, including adult GH deficiency and HIV lipodystrophy, as well as broader patient populations involving a wide variety of metabolic/endocrine diseases. Relative to GH injections, GHRH therapy produces a more physiological response, thereby minimizing safety and tolerability issues associated with chronic, excess GH replacement.

(Filing, 10-Q, Soligenix, MAY 3, 2013, View Source [SID:1234506508])

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