Corporate presentation

On September 8, 2023 Portage biotech presented its corporate presentation (Presentation, Portage Biotech, SEP 8, 2023, View Source [SID1234635030]).

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PharmaMar to present new data on lurbinectedin at the IASLC 2023 World Lung Cancer Congress

On September 8, 2023 PharmaMar (MSE:PHM) reported five abstracts to be presented at the IASLC World Lung Cancer Congress 2023 on its compound Zepzelca (lurbinectedin) (Press release, PharmaMar, SEP 8, 2023, View Source [SID1234635029]).

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Among the most important studies to be made public are the following: "Efficacy of Platinum after Lurbinectedin + DOX or Topotecan/CAV in Sensitive Relapsed SCLC Patients in the ATLANTIS Trial". Patients with platinum-sensitive, relapsed Small Cell Lung Cancer (SCLC) who received platinum re-challenge immediately after lurbinectedin + doxorubicin showed longer survival compared to those who received it after topotecan/CAV, thereby suggesting that giving lurbinectedin as second line to platinum-sensitive, relapsed SCLC patients does not affect the efficacy of subsequent platinum re-challenge and could extend the platinum-free interval and improve patient survival.

"Efficacy of Platinum Given after Lurbinectedin in Sensitive Relapsed SCLC Patients". These results suggest that lurbinectedin may effectively extend the platinum-free interval while maintaining the possibility of platinum re-challenge, leading to improved outcomes for patients with relapsed SCLC.

As part of the conclusion of the last two posters, Dr Ali Zeaiter, VP and Head of Clinical Development at PharmaMar says: "the effect of platinum re-challenge after lurbinectedin given as monotherapy or in combination with doxorubicin is similar to that previously reported with platinum re-challenge as second line therapy in platinum-sensitive patients (Baize et al., 2020). This supports that lurbinectedin is an alternative second line treatment option to platinum re-challenge for patients with platinum-sensitive relapsed SCLC".

"Effectiveness and Safety Profile of Lurbinectedin in Second-Line Small Cell Lung Cancer: A Real-World Data Study". The safety and effectiveness outcomes of lurbinectedin in relapsed Small Cell Lung Cancer (SCLC) in the real world were generally consistent with those seen in the phase II trial. In addition, the rates of neutropenia, thrombocytopenia, anemia and febrile neutropenia tended to be lower than what was observed in the basket trial.

"Real-world Safety and Dosing of Lurbinectedin-Treated Patients with Small Cell Lung Cancer: Jazz EMERGE 402 Preliminary Analysis." The study continues to enroll a broader population of SCLC patients than the collective Phase II trial that supported FDA approval. The real-world safety profile of lurbinectedin in this analysis was generally consistent with those reported in the collective trial, with no new safety events. The prophylactic use of G-CSF likely contributed to the low rates of neutropenia reported.

Lurbinectedin’s abstracts at the IASCL 2023 World Lung Cancer Congress
PRODUCT TITLE LEAD AUTHOR ABSTRACT
Zepzelca (lurbinectedin) Effectiveness and Safety Profile of Lurbinectedin in Second-Line Small Cell Lung Cancer A.K. Ganti ABSTRACT: P2.17-02 POSTER SESION: Small Cell Lung Cancer and Neuroendocrine Tumors – Relapse and Salvage Therapy
Efficacy of Platinum after Lurbinectedin + DOX or Topotecan/CAV in Sensitive Relapsed SCLC Patients in the ATLANTIS Trial Alejandro Navarro ABSTRACT: P2.17-06 POSTER SESION: Small Cell Lung Cancer and Neuroendocrine Tumors – Relapse and Salvage Therapy
Real-world Safety and Dosing of Lurbinectedin-Treated Patients with Small Cell Lung Cancer: Jazz EMERGE 402 Preliminary Analysis B. Halmos ABSTRACT: P2.17-07 POSTER SESION: Small Cell Lung Cancer and Neuroendocrine Tumors – Relapse and Salvage Therapy
Efficacy of Platinum Given after Lurbinectedin in Sensitive Relapsed SCLC Patients J.M Trigo ABSTRACT: EP13.07-06 POSTER SESION: Small Cell Lung Cancer and Neuroendocrine Tumors – Relapse and Salvage Therapy
Cost- Effectiveness Modeling of Lurbinectedin As a Second-line Therapy in Patients with Small Cell Lung Cancer Wayne Su

Pioneering gene therapies for patients in need

On September 8, 2023 Genprex presented its corporate presentation (Presentation, Genprex, SEP 8, 2023, View Source [SID1234635028]).

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Corporate Overview

On September 8, 2023 Foghorn therapeutics presented its corporate presentation (Presentation, Foghorn Therapeutics, SEP 8, 2023, View Source [SID1234635027]).

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Coherus Completes Surface Oncology Acquisition

On September 8, 2023 Coherus BioSciences, Inc. (Coherus, Nasdaq: CHRS) reported the closing of the previously announced acquisition of Surface Oncology, Inc. (Surface or Surface Oncology), a clinical-stage immuno-oncology (I-O) company developing next-generation immunotherapies that target the tumor microenvironment (Press release, Coherus Biosciences, SEP 8, 2023, View Source [SID1234635026]). As a result of the acquisition, Coherus’ novel I-O pipeline now includes four differentiated clinical-stage assets:

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Toripalimab, a late-stage, anti-PD-1 monoclonal antibody candidate under BLA review for the potential treatment of advanced recurrent or metastatic nasopharyngeal carcinoma (NPC);
Casdozokitug (SRF388 or casdozo), a novel, first-in-class IL-27-targeted antibody currently being evaluated in Phase 2 clinical trials in lung cancer and liver cancer;
CHS-114 (SRF114), a highly selective, competitively positioned, ADCC-enhanced CCR8-targeted antibody currently in a Phase 1/2 study as a monotherapy in patients with advanced solid tumors; and
CHS-006, a TIGIT-targeted antibody currently in a Phase 1/2 study in combination with toripalimab in patients with advanced solid tumors.
"The addition of the first-in-class IL-27 targeted antibody, casdozo, and the potential best-in-class CCR8 targeted antibody CHS-114, marks Coherus’ transition to a next-generation immuno-oncology company focused on the tumor microenvironment," said Denny Lanfear, Chairman and Chief Executive Officer of Coherus. "We will now focus our development efforts on delivering breakthrough survival benefits for cancer patients, beyond the efficacy seen with existing chemotherapy plus checkpoints regimens. Toripalimab combinations with these two new agents have the potential to expand tori use into highly prevalent tumor types including NSCLC and head and neck cancer, where it has already consistently shown clinically meaningful activity."

At the closing of the acquisition, Coherus issued 0.1960 shares of its common stock per share of outstanding Surface common stock and certain outstanding Surface employee equity awards (which exchange ratio was calculated based on a $5.2831 per share price of Coherus common stock) for a total value equal to approximately $66.9 million, the sum of $40 million plus Surface’s net cash at closing of the transaction of $26.9 million. Surface shareholders also received contingent value rights (CVRs) for 70% of milestone and royalty-based value of existing programs with Novartis (NZV930) and GSK (GSK4381562), as well as for 25% of upfront payments made pursuant to potential ex-US licensing agreements for CHS-114 and 50% of upfront payments made pursuant to potential ex-US licensing agreements for casdozokitug, subject to certain deductions as set forth in the contingent value rights agreement. Amounts under these CVRs are payable for a period of ten years following the closing of this transaction. As a result of the acquisition, Surface has become a wholly owned subsidiary of Coherus and the common stock of Surface will no longer be listed for trading on the Nasdaq Capital Market, effective as of prior to market open on September 8, 2023.

Truist Securities acted as financial advisor, and Arnold & Porter Kaye Scholer LLP and Latham & Watkins LLP acted as legal advisors to Coherus. Wedbush Securities Inc. acted as exclusive strategic financial advisor, and Goodwin Procter LLP acted as legal advisor to Surface.