Cerus Corporation to Participate in Stifel 2021 Virtual Healthcare Conference

On November 8, 2021 Cerus Corporation (Nasdaq: CERS) reported that William ‘Obi’ Greenman, Cerus’ president and chief executive officer, and Kevin D. Green, Cerus’ chief financial officer, are scheduled to participate in the Stifel 2021 Virtual Healthcare Conference on Monday, November 15, 2021 at 4:40 p.m. ET (Press release, Cerus, NOV 8, 2021, View Source [SID1234594714]).

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A live webcast of the events will be available on the Investor Relations page of the Cerus web site at View Source A replay will be available for approximately two weeks following the completion of the event.

SITC 2021, NI-2601 & NI-2901 bispecific antibody programs

On November 8, 2021 Light Chain Bioscience reported to have Xavier Chauchet attend in-person the Society for Immunotherapy of Cancer (SITC) (Free SITC Whitepaper) Annual Meeting on November 10-14, 2021 in Washington DC (Press release, Light Chain Bioscience, NOV 8, 2021, View Source [SID1234594730]).

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Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

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Xavier will present our innovative and differentiating CD47xPD-L1 bispecific antibodies for a simultaneous blockade of PD-1/PD-L1 and CD47/SIRPa immune checkpoint axes, NI-2601 and NI-2901. The programs are currently in late discovery phase and clinical lead candidates have been identified.

The poster entitled "CD47xPD-L1 bispecific antibodies for cancer therapy" (#265) will be exposed and presented on Nov. 12 between 9:55-10:10 a.m., 12:40-14:10 p.m., 4:35-4:50 p.m. and 7:00-8:30 p.m. and available on the SITC (Free SITC Whitepaper) virtual meeting ePoster platform from 7 a.m. on Friday, Nov.12.

Biocept to Report Third Quarter 2021 Financial Results and Host Investor Conference Call on November 15, 2021

On November 8, 2021 Biocept, Inc. (Nasdaq: BIOC), a leading provider of molecular diagnostic assays, products and services, reported that it will release financial results for the three and nine months ended September 30, 2021 after the market closes on Monday, November 15, 2021 (Press release, Biocept, NOV 8, 2021, View Source [SID1234594747]). The Company will host an investor conference call to discuss the results and answer questions at 4:30 p.m. Eastern time (1:30 p.m. Pacific time).

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Discover why more than 1,500 members use 1stOncology™ to excel in:

Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

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Those who choose not to pre-register can access the live conference call by dialing the following and requesting the Biocept call:

A live webcast of the call will be available at https://ir.biocept.com/. The webcast will be archived for 90 days.

A replay of the conference call will be available for 48 hours following the conclusion of the call by dialing (877) 344-7529 for domestic callers, (855) 669-9658 for Canadian callers, or (412) 317-0088 for other international callers, and entering the replay access code 10161580.

Ziopharm Oncology Reports Third Quarter 2021 Financial Results and Provides Business Update

On November 8, 2021 Ziopharm Oncology, Inc. ("Ziopharm" or the "Company") (Nasdaq: ZIOP), reported financial results for the third quarter ended September 30, 2021 and provided a business update (Press release, Ziopharm, NOV 8, 2021, View Source [SID1234594795]).

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Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

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"I am impressed by the quality and dedication of our team at Ziopharm who all are diligently working to transform our cutting-edge scientific research into meaningful clinical progress. Last quarter we made the decision to restructure the organization and focus our efforts on advancing our differentiated TCR-T library towards the clinic," said Kevin S. Boyle, Sr., Chief Executive Officer at Ziopharm Oncology. "We are making excellent progress to operationalize our in-house cGMP clinical production unit. We completed the necessary engineering and process qualification runs in October and remain committed to begin treating patients in the first half of 2022. Our team is executing on this disciplined strategy to bring value to our stakeholders and improve the lives of cancer patients."

Recent Developments and Upcoming Milestones:

TCR-T Library Clinical Program: Ziopharm’s planned Phase 1/2 TCR-T Library study will be a basket trial and enroll patients with non-small cell lung cancer, colorectal, endometrial, pancreatic, ovarian and cholangiocarcinoma where a matching neoantigen TCR/HLA pairing is available in the Company’s TCR-T library. Using the Company’s Sleeping Beauty transposon/transposase technology, patients will be infused with autologous T-cells that have been engineered to express T-cell receptors that are reactive against mutated neoantigens. Patients will be enrolled in one of three progressing TCR-T cells dose levels. The primary endpoint of the initial phase of the study will be to determine the Maximum Tolerated Dose (MTD) or optimal TCR-T cells dose. Ziopharm continues to expect to dose the first patient in the TCR-T Library Phase 1/2 clinical trial in the first half of 2022.

cGMP clinical production unit (CPU): Ziopharm continues to develop its in-house cGMP CPU in Houston, TX, which is expected to operationalize in the first half of 2022 to support the manufacturing of TCR-T therapies for Ziopharm’s Phase 1/2 TCR-T library trial. In the third quarter, the Company continued to make progress in establishing these manufacturing capabilities, and in October, completed engineering and process qualification runs in the CPU.

Expanding library of TCRs through a robust R&D discovery engine: The Company continues to qualify new TCRs using its Sleeping Beauty technology to further expand the potential utility and applicable patient population for its TCR-T Library. Ziopharm expects to file an amended investigational new drug (IND) application for its TCR-T Library clinical program in the next few months to include four additional TCRs.

Corporate Updates:

Completed strategic restructuring: In September 2021, Ziopharm announced a greater than 50% reduction in personnel, enabling the Company to extend its cash runway and prioritize advancing its lead TCR-T library program towards the clinic.

Leadership Appointments: In October 2021, Ziopharm announced that Michael Wong has been appointed Vice President, Finance and Principal Accounting Officer. Mr. Wong brings over 15 years of experience to Ziopharm. Most recently he was Director of Technical Accounting at a large public company.

Third Quarter Ended September 30, 2021 Financial Results:

Research and Development Expenses: Research and development expenses were $14.5 million for the quarter ended September 30, 2021, as compared to $14.0 million for the same period in 2020, an increase of approximately 4%. The increase in research and development expense was primarily due to a $2.2 million charge recognized during the third quarter of 2021 related to our strategic restructuring announced on September 27. The increase was primarily offset by $1.6 million in reduced trial and consulting costs.

General and Administrative Expenses: General and administrative expenses were $8.2 million for the quarter ended September 30, 2021, as compared to $6.4 million for the same period in 2020, an increase of approximately 29%. The increase in general and administrative expenses was primarily due to $1.3 million in employee related severance charges in association with our September 2021 strategic restructuring recognized during the third quarter of 2021 and an increase of $0.8 million related to consulting service costs. The increases were partially offset by a $0.1 million decrease in salary and employee related costs.

Net Loss: Net loss was $22.7 million, or $0.11 net loss per share, for the quarter ended September 30, 2021, as compared to a net loss of $20.3 million, or $0.10 net loss per share, for the same period in 2020. The increase was primarily due to the severance charge of $3.5 million related to our strategic restructuring.

Cash and Cash Equivalents: As of September 30, 2021, Ziopharm had approximately $91.7 million in cash and cash equivalents. Given its current development plans and continued cost management efforts, the Company anticipates its cash runway will extend into the second quarter of 2023.

Conference Call and Webcast

Ziopharm will host a conference call and webcast today, November 8, 2021 at 4:30pm ET. Participants should dial 877-451-6152 (United States) or 201-389-0879 (International) with the conference code 13724384. A live webcast may be accessed using the link here, or by visiting the "Investors" section of the Ziopharm website at www.ziopharm.com. After the live webcast, the event will be archived on Ziopharm’s website for approximately 90 days after the call.

RedHill Biopharma and South Korea’s Kukbo Co. Announce a Strategic Investment of Up To $10 Million in RedHill

On November 8, 2021 RedHill Biopharma Ltd. (Nasdaq: RDHL) ("RedHill" or the "Company"), a specialty biopharmaceutical company, reported that it has entered into a strategic agreement with Kukbo Co. Ltd. (Kospi: 001140) ("Kukbo"), a South Korean corporation, for the sale of RedHill’s American Depositary Shares ("ADSs") in a private placement of up to $10 million at a 20% premium to the prior 30 trading days’ volume weighted average price ("VWAP") (Press release, RedHill Biopharma, NOV 8, 2021, View Source [SID1234595344]).

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Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

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Kukbo’s strategic investment in RedHill is to be made in two tranches, with the first tranche of $5 million already paid and the second tranche of $5 million to follow within six months, subject to satisfaction of certain conditions. As part of the first tranche, RedHill is to issue 827,586 ADSs at a purchase price of $6.04, representing a 20% premium based on the VWAP of RedHill’s ADS on NASDAQ over the 30 trading days ending on the effective date. All ADSs are to be issued with a 180-day transfer restriction.

In addition, under the terms of the agreement, RedHill has agreed to grant Kukbo a right of first offer, for a period of six months, for a license with respect to one or more of RedHill’s late-stage clinical assets, opaganib, RHB-107 (upamostat)1 and Talicia, for one or more of the territories of South Korea, Japan, Indonesia, Vietnam, Thailand and Malaysia. Kukbo has the right to elect not to purchase the ADSs in the second tranche if no such license agreement is executed within six months of the closing of the first tranche.

Dror Ben-Asher, RedHill’s CEO said: "We are rapidly advancing with opaganib’s COVID-19 data package submissions to regulators in several territories including the U.S., EU and others, ahead of planned regulatory advice. We are pleased with the addition of Kukbo as a committed strategic investor and look forward to evaluating opportunities for opaganib, RHB-107 and Talicia in South Korea and other territories in Asia where large unmet medical needs exist."

"As Kukbo proceeds in its planned strategic expansion into healthcare, we believe that RedHill’s opaganib, RHB-107 and Talicia, if approved, hold substantial promise in South Korea and other Asian countries and are eager to leverage our local expertise and network in those territories," said Hyun Ha, Kukbo’s CEO.

Nexpedia Holdings Co., Ltd. and Network 1 Financial Securities, Inc. facilitated the introduction between the parties.

The securities to be sold in the private placement have not been registered under the Securities Act of 1933, as amended (the "Securities Act"), or any state or other applicable jurisdiction’s securities laws, and may not be offered or sold in the United States absent registration or an applicable exemption from the registration requirements of the Securities Act and applicable state or other jurisdictions’ securities laws.

This press release shall not constitute an offer to sell or the solicitation of an offer to buy these securities, nor shall there be any offer, solicitation, or sale of these securities in any jurisdiction in which such offer, solicitation or sale would be unlawful.