Janux Therapeutics to Present Virtually at Upcoming Investor Conferences

On November 8, 2021 Janux Therapeutics, Inc. (Nasdaq: JANX) (Janux), a biopharmaceutical company developing a broad pipeline of novel immunotherapies by applying its proprietary technology to its Tumor Activated T Cell Engager (TRACTr) and Tumor Activated Immunomodulator (TRACIr) platforms, reported that Janux management will participate in fireside chats at two upcoming virtual investor conferences (Press release, Janux Therapeutics, NOV 8, 2021, View Source [SID1234594748]):

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Cowen’s 5th Annual IO Next Summit
Forum: Fireside Chat
Date: Monday, November 15th, 2021
Time: 12:15-12:35 p.m. ET

Evercore ISI 4th Annual Health CONx Virtual Conference
Forum: Fireside Chat
Date: Thursday, December 2nd, 2021
Time: 2:40 – 3:00 p.m. ET

Both fireside chats and subsequent archived replays may be accessed via the Investors & Media section of Janux’s website. An archived replay of both webcasts will be available on the website for approximately 90 days following the presentation.

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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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.

Bicara Therapeutics to Present at Upcoming November Investor Conferences

On November 8, 2021 Bicara Therapeutics, a clinical-stage biotechnology company developing dual-action biologics designed to elicit a potent and durable immune response in the tumor microenvironment, reported that company leadership will participate in two upcoming virtual investor conferences in November (Press release, Bicara Therapeutics, NOV 8, 2021, View Source [SID1234594746]):

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Stifel 2021 Virtual Healthcare Conference
Format: Live presentation
Date: Monday, November 15, 2021
Time: 10:40 – 11:10 a.m. ET

Piper Sandler 33rd Annual Virtual Healthcare Conference
Format: On-demand presentation
Date: Monday, November 22, 2021
Time: 10:00 a.m. ET

NeoImmuneTech Announces First Patient Dosed in Phase 2 Study of NT-I7 (efineptakin alfa) in Combination with PD-L1 Checkpoint Inhibitor in Frontline Locally Advanced or Metastatic Non-Small Cell Lung Cancer

On November 8, 2021 NeoImmuneTech, Inc. (KOSDAQ: 950220), a clinical-stage T cell-focused biopharmaceutical company, reported that the first patient has been dosed in a Phase 2 study evaluating NT-I7 (efineptakin alfa), a novel long-acting human interleukin-7 (IL-7), in combination with atezolizumab (Tecentriq) as a first-line (1L) treatment for patients with PD-L1-expressing, locally advanced or metastatic non-small cell lung cancer (NSCLC) (Press release, NeoImmuneTech, NOV 8, 2021, View Source [SID1234594745]).

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NSCLC accounts for approximately 85% of all cases of lung cancer. Lung cancer is the second most commonly diagnosed cancer worldwide – in 2020, an estimated 2.2 million new cases of lung cancer were diagnosed globally, accounting for approximately 11.4% of the global cancer burden. An estimated 1.8 million lung cancer deaths occurred in 20201. Atezolizumab has shown clinically meaningful benefit in various types of lung cancer, with six currently approved indications in the US. Atezolizumab now has five approved indications in NSCLC in the US, including as a single agent or in combination with targeted therapies and/or chemotherapies. It was also the first approved cancer immunotherapy for the first-line treatment of adults with extensive-stage small cell lung cancer (SCLC) in combination with carboplatin and etoposide (chemotherapy) and the first approved cancer immunotherapy for adjuvant NSCLC.

"Following preclinical studies which showed promising evidence that adding NT-I7 to atezolizumab increased the anti-tumor activity, we are pleased to have commenced this Phase 2 trial," said Se Hwan Yang, Ph.D., President and Chief Executive Officer of NIT. "NT-I7’s T cell-amplifying properties may make it an excellent partner in combination with a checkpoint inhibitor, like atezolizumab, and this study could bring us closer to a new chemo-free treatment option for patients with PD-L1-expressing NSCLC. We look forward to evaluating how the addition of NT-I7 impacts the effects of single-agent atezolizumab in frontline locally advanced or metastatic NSCLC."

This multicenter Phase 2 study will evaluate the efficacy and safety of the combination therapy. Roche will supply NeoImmuneTech with atezolizumab for the clinical trial. More information can be found at www.neoimmunetech.com or www.clinicaltrials.gov, identifier: NCT04984811.

Tecentriq (atezolizumab) is a registered trademark of Genentech, a member of the Roche Group.

About NT-I7

NT-I7 (efineptakin alfa) is the only clinical-stage long-acting human IL-7, and is being developed for oncologic and immunologic indications, in which T cell amplification and enhanced functionality may provide clinical benefit. IL-7 is a fundamental cytokine for naïve and memory T cell development and for sustaining immune response to chronic antigens (as in cancer) or foreign antigens (as in infectious diseases). In clinical trials to date, NT-I7 has exhibited favorable PK/PD and safety profiles, both as a monotherapy and in combination with other anticancer treatments. NT-I7 is being studied in multiple clinical trials in solid tumors and as a vaccine adjuvant. Studies are being planned for testing in hematologic malignancies, additional solid tumors and other immunology-focused indications.

TYME Technologies, Inc. Provides Business Update and Announces Second Fiscal Quarter 2022 Financial and Operating Results

On November 8, 2021 TYME Technologies, Inc. (Nasdaq: TYME) (the Company or TYME), an emerging biotechnology company developing cancer metabolism-based therapies (CMBTs), reported financial and operating results for its second fiscal quarter ended September 30, 2021 (Press release, TYME, NOV 8, 2021, View Source [SID1234594744]).

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Second Fiscal Quarter 2022 Business and Recent Highlights:

Commenced enrollment and dosed first patient in OASIS breast cancer trial, a multicenter Phase II single-arm, open-label study examining SM-88 with methoxsalen, phenytoin, and sirolimus (MPS) in patients with metastatic disease who have received two prior hormonal therapies. The trial is being conducted by Georgetown University (NCT04720664) at five MedStar Health hospitals. (MedStar Health is Georgetown’s academic clinical partner).
Five new sites planned to be added in early 2022 with an additional 10 sites expected by the end of 2022, on top of the 15 already participating (for a total of 30 sites), in the Precision Promise trial, a Phase II/III randomized adaptive trial in metastatic pancreatic cancer sponsored by the Pancreatic Cancer Action Network (PanCAN). These sites are among the top research institutions in the country for pancreatic cancer treatment.
The HOPES Sarcoma trial, an investigator-sponsored trial, had a meaningful increase in the rate of enrollment during the quarter. We anticipate completing trial enrollment by the end of the first half of calendar year 2022.
Launched preclinical initiative with Evotec to evaluate the potential of expanding SM-88 platform to other targeted indications.
Announced plans to explore the development of a Tyrosine-based tumor targeted technology and the receipt of a patent on such platform.
"Our second quarter was a period of significant action at TYME as we continued to implement our strategic imperatives. We commenced the OASIS breast cancer study with the first patient dosed in late September, and initiated our preclinical work, including our all-important biomarker research. We believe this will provide us with a better understanding of how best to address treatment opportunities. Our existing trials are also progressing, as planned. PanCAN’s Precision Promise trial is in the process of seeking five new sites early next year with plans to add 10 more by the end of the year and enrollment continues in our HopES sarcomas study. This is particularly noteworthy given how difficult it is to recruit patients with this ultra-rare sarcoma. Finally, we began early discovery work on a tyrosine-based tumor targeted technology platform," stated Richie Cunningham, Chief Executive Officer of TYME.

"Given all the positive momentum, these are exciting times at TYME, and we are in a strong financial position to advance these programs. We look forward to sharing information on our progress in the upcoming quarters," concluded Cunningham.

Second Fiscal Quarter 2022 Financial Results

As of the quarter ended September 30, 2021, the Company had approximately $96.6 million in cash and marketable securities, compared to $101.5 million as of the quarter ended June 30, 2021. TYME’s operational cash burn rate for the second quarter of fiscal year 2022 was $5.0 million compared to $6.0 million for the first quarter and $6.6 million for the second quarter of fiscal year 2021.

The burn rate was below the Company’s previous guidance and reflected expenses associated with ongoing clinical trials in pancreatic cancer (Precision Promise), breast cancer (Oasis), and sarcoma cancers (HopES), as well as reduced costs associated with our discontinued pancreatic cancer trial, 88-Panc-Part II. TYME continues to anticipate that its quarterly cash usage or "cash burn rate" will range from $6.0 to $8.0 million for the remaining quarters of fiscal year 2022, based on costs associated with the Company’s active clinical trials, the ongoing and close out activities related to our discontinued pancreatic cancer study, our pre-clinical studies in biomarker and mechanism of action research of SM-88, and TYME-19 pre-clinical studies.

Net loss was $5.6 million for the quarter ended September 30, 2021, or ($0.03) per basic and diluted share, as compared to a net loss of $6.9 million for the quarter ended September 30, 2020, or ($0.05) per basic and diluted share. The decrease reflected lower ongoing trial costs primarily due to the discontinued TYME—88- Panc Part 2 trial.

After adjusting for the change in fair value of warrant liability, and amortization of employee, director and consultant stock options, adjusted net loss for the three months ended September 30, 2021, was $5.3 million, or ($0.03) per share, compared to adjusted net loss of $6.5 million, or ($0.04) per share, for the three months ended September 30, 2020. Adjusted net loss and adjusted net loss per share are non-GAAP measures. See "Use of Non-GAAP Measures" below for a reconciliation to the comparable GAAP measures.

TYME has reported its full financial results for the quarter ended September 30, 2021, in the Company’s Form 10-Q filed with the Securities and Exchange Commission ("SEC"). TYME’s 10-Q is located in the SEC filings section of the Company’s website.

Conference Call and Webcast Details

The webcast will be accessible on the Events & Presentations page of the Investors section of the TYME website, tymeinc.com, and will be archived for 90 days following the event.

Use of Non-GAAP Measures

Adjusted net loss and adjusted net loss per share as presented in this report are non-GAAP measures. The adjustments relate to the change in fair value of warrant liability, amortization of employees, directors and consultants stock options and gain on warrant exchange. These financial measures are presented on a basis other than in accordance with U.S. generally accepted accounting principles ("Non-GAAP Measures"). In the reconciliation tables that follow, we present adjusted net loss and adjusted net loss per share, reconciled to their comparable GAAP measures, net loss and net loss per share. These items are adjusted because they are not operational or because they are significant noncash charges and management believes these adjustments are meaningful to understanding the Company’s performance during the periods presented. These Non-GAAP Measures should be considered a supplement to, not a substitute for, or superior to, the corresponding financial measures calculated in accordance with GAAP. Our definitions of adjusted net loss and adjusted loss per share may not be comparable to similar measures reported by other companies.