Innate Pharma Files Its 2021 Universal Registration Document (Document d’enregistrement universel) and 2021 Annual Report on Form 20-F

On April 5, 2022 Innate Pharma SA (Euronext Paris: IPH; Nasdaq: IPHA) ("Innate" or the "Company") reported the filing of its 2021 Universal Registration Document (Document d’enregistrement universel) for the year ending December 31, 2021 with the French market authority "Autorité des Marchés Financiers" ("AMF") on April 4, 2022 (Press release, Innate Pharma, APR 5, 2022, View Source [SID1234611455]). It can be downloaded (in French) on the Company’s website and on the AMF’s website.

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The Company also announced today the filing of its annual report on Form 20-F for the year ending December 31, 2021 with the United States Securities and Exchange Commission ("SEC"). It can be also be accessed on the Company’s website and on the SEC’s website.

AffyImmune Therapeutics to Present Poster at American Association for Cancer Research Annual Meeting

On April 5, 2022 AffyImmune Therapeutics, Inc., a clinical stage biotechnology company using its Tune & Track platform to develop CAR T cells for the treatment of solid cancers, reported that it will present an abstract in a poster session at the 2022 American Association for Cancer Research (AACR) (Free AACR Whitepaper) Annual Meeting in New Orleans, Louisiana, which is being held April 8 – 13 (Press release, AffyImmune Therapeutics, APR 5, 2022, View Source [SID1234611454]). Presented findings will highlight research using AffyImmune’s Tune & Track platform for the affinity tuning of the interaction between CAR T cells and cancer antigen, tracking of CAR T cells in real-time, and armoring of CAR T cells with cytokines.

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Details of the abstract and poster are as follows:
Title: Focused IL-12 cytokine delivery enhances function of affinity-tuned and real-time tracked ICAM-1-specific CAR T cells in solid tumors
Presenting Author: Michael Gallagher, PhD, Scientist
Session Category: Adoptive Cell Therapy 1
Poster Number: 558/12
Abstract Number: 4978
Presentation Type: Poster
Date, Time, and Location: Sunday, April 10, 1:30 – 5:00 pm, Poster Section 36

Iovance Biotherapeutics Announces Regulatory and Clinical Updates for Lifileucel in Melanoma

On April 5, 2022 Iovance Biotherapeutics, Inc. (NASDAQ: IOVA), a late-stage biotechnology company developing novel T cell-based cancer immunotherapies, reported that the U.S. Food and Drug Administration (FDA) has provided feedback on April 1, 2022 regarding Iovance’s proposed matrix of potency assays for its upcoming Biologics License Application (BLA) for lifileucel in metastatic melanoma (Press release, Iovance Biotherapeutics, APR 5, 2022, View Source [SID1234611453]). Iovance received positive feedback from the FDA on both its potency assay matrix and its proprietary cell co-culture assay included in the potency assay matrix. Based on this response, Iovance expects to request a pre-BLA meeting in July 2022 and to complete a BLA submission for lifileucel by August 2022.

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Frederick Vogt, Ph.D., J.D., Interim President and Chief Executive Officer of Iovance, stated, "The favorable feedback received from the FDA on our potency assays and assay matrix brings Iovance a step closer to our submission of a BLA for lifileucel in metastatic melanoma. We look forward to bringing lifileucel to the market quickly to offer melanoma patients a new option following anti-PD-1 therapy."

In addition, Iovance reported plans to open a Phase III study for lifileucel in combination with pembrolizumab for the treatment of immune checkpoint inhibitor (ICI) naïve frontline metastatic melanoma in late 2022. Updated data from the combination cohort of lifileucel and pembrolizumab in ICI naïve patients (Cohort 1A in the IOV-COM-202 study, n=12) demonstrated an overall response rate (ORR) of 67%. Eight out of 12 patients had a confirmed objective response per RECIST 1.1, including three complete responses and five partial responses. Six of the eight responders had ongoing response at the time of the last data cut, and five responders had a duration of response of more than one year. The FDA previously granted Fast Track Designation for lifileucel in combination with pembrolizumab for the treatment of ICI naïve metastatic melanoma based on the unmet medical need and potential advantages for this combination over available care.

Management will host a conference call and live audio webcast to discuss these updates at 8:00 a.m. Eastern time on April 6, 2022. To participate in the conference call, please dial 1-844-646-4465 (domestic) or 1-615-247-0257 (international) and reference the access code 3734669. The live webcast can be accessed in the Investors section of the Company’s website at www.iovance.com. The archived webcast will also be available for one year in the Investors section at www.iovance.com.

Shattuck Labs Announces Participation in Upcoming 21st Annual Needham Virtual Healthcare Conference

On April 5, 2022 Shattuck Labs, Inc. (NASDAQ: STTK), a clinical-stage biotechnology company pioneering the development of bi-functional fusion proteins as a new class of biologic medicine for the treatment of patients with cancer and autoimmune disease, reported that company management will participate in the 21st Annual Needham Virtual Healthcare Conference being held April 11-14, 2022 (Press release, Shattuck Labs, APR 5, 2022, View Source [SID1234611452]).

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Presentation Details

Conference: 21st Annual Needham Virtual Healthcare Conference
Format: Fireside chat with covering analyst Gil Blum, Ph.D.
Presenters: Taylor Schreiber, M.D., Ph.D., Shattuck’s Chief Executive Officer and Andrew Neill, M.B.A., Shattuck’s Chief Financial Officer
Date: April 11, 2022
Time: 1:30 p.m. ET

A live webcast of the presentation will be available on the Events & Presentations section of the Company’s website. A replay of the webcasts will be archived for up to 90 days following the presentation date.

SELLAS Life Sciences Provides Business Update and First Quarter 2022 Highlights

On April 5, 2022 SELLAS Life Sciences Group, Inc. (NASDAQ: SLS) ("SELLAS" or the "Company"), a late-stage clinical biopharmaceutical company focused on the development of novel therapies for a broad range of cancer indications, reported a business update and overview of activity in the first quarter of 2022 (Press release, Sellas Life Sciences, APR 5, 2022, View Source [SID1234611451]).

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"The first quarter of 2022 has been transformative for SELLAS as we have significantly enhanced our clinical pipeline with the in-license from GenFleet Therapeutics (Shanghai), Inc. ("GenFleet") of global rights outside of Greater China for GFH009, a highly selective small molecule cyclin-dependent kinase 9 ("CDK9") inhibitor. At the same time, we have continued to progress our lead asset, galinpepimut-S ("GPS"), which is currently being tested in clinical trials for acute myeloid leukemia ("AML"), malignant pleural mesothelioma ("MPM") and relapsed/refractory metastatic ovarian cancer," said Angelos M. Stergiou, MD, ScD. h.c., President and Chief Executive Officer of SELLAS. "We also strengthened our balance sheet with the closing of a public offering, underwritten by SVB Leerink and Cantor, which will support the continued development of GPS and our ongoing and planned studies for GFH009. We view the addition of GFH009 as a strategic fit to our overall clinical development plans."

Dr. Stergiou continued, "GFH009 provides us with an opportunity to expand further into the market for AML therapeutics covering not only the maintenance phase of the disease, which is the indication being studied for GPS in the REGAL trial, but also active disease by combining GFH009 with venetoclax and azacitidine. GFH009 has shown a strong synergy with venetoclax in preclinical models, and we believe it has the potential to improve response to venetoclax or possibly convert resistance to venetoclax into a response. Furthermore, we have an opportunity with GFH009 to address additional indications and tumor types, including the very important pediatric market of soft tissue sarcomas – positive results from this program could ultimately provide the basis for a rare pediatric disease priority voucher. Additionally, GenFleet plans to conduct numerous Phase 2 clinical trials for hematological malignancies in China. The data generated by these trials will effectively help us to analyze and identify additional indications in which to launch pivotal studies in our own territories. This parallel development in different indications allows both companies to leverage a much broader body of both safety and efficacy data thus potentially significantly accelerating clinical development."

"As we continue to progress toward commercialization with GPS, we were thrilled to announce that Robert Francomano joined the SELLAS team in March as Chief Commercial Officer. Robert brings to SELLAS more than 25 years of biopharmaceutical experience, with the majority of time spent in the hematology/oncology therapeutic area, making him a strong addition to our management team," Dr. Stergiou concluded.

Pipeline Update:

Galinpepimut-S (GPS)

Phase 3 REGAL Study: The Company is continuing to activate and enroll patients in additional sites in the United States, Europe, and Asia. As has been the case with many of its peer companies, the Company has continued to observe that COVID-19 related delays have impacted its projected timeline for the REGAL study. Under the Company’s current planning assumptions, which take into account the Company’s best estimates of potential delays due to COVID-19 as well as input by its external statisticians and experts, the Company believes that enrollment for the REGAL study will be completed in late 2022 or early in the first quarter of 2023 and the planned interim analysis will occur by the end of the first half of 2023, provided that its statistical assumptions and assumptions regarding the impact of COVID-19 on the operations of clinical sites as well as the duration of the pandemic remain unchanged. Because this analysis is event driven, it may become available at a different time than currently expected.

Phase 1/2 GPS Study in Combination with Merck’s KEYTRUDA: In February 2022, the Company completed enrollment in the Phase 1/2 clinical trial of GPS in combination with Merck’s anti-PD-1 therapy, KEYTRUDA (pembrolizumab), in second or third line Wilms Tumor-1 (WT1)(+) relapsed or refractory metastatic ovarian cancer. Data from 15 patients will be examined by mid-2022, with final data analysis for all evaluable patients expected by the end of 2022.

Phase I GPS Study in China: In March 2022, an IND application to initiate the first clinical trial in China for GPS was approved by China’s National Medical Products Administration which triggered a milestone payment of $1 million, expected to be received by the Company in the second quarter of 2022. The IND, for a small Phase I clinical trial investigating safety, was submitted by SELLAS’ partner in China, 3D Medicines Inc. ("3D Medicines"). 3D Medicines expects to initiate the trial by mid-2022.
Manufacturing Improvements : In the fourth quarter of 2021, the Company’s contract manufacturer for GPS, Lyophilization Services of New England, Inc. (LSNE), manufactured a new regulatory standard drug product batch which entailed further process improvements, which were agreed upon by the FDA. The new manufacturing batch met all the release criteria and, to date, has shown favorable stability data on already known long-term conditions (-20°C) as well as newly accelerated conditions (5°C and 25°C). Both long-term and accelerated stability data are monitored to confirm that all drug product parameters are within the acceptance criteria. This optimized batch, based on the data to date, may ultimately allow for GPS to be stored in 5°C to 25°C conditions versus -20°C, which would be more optimal for supply chain and logistical reasons.

New Patent Allowance: In February 2022, the U.S. Patent and Trademark Office issued a Notice of Allowance for a patent application covering certain WT1-targeting peptides, in combination with other molecules such as other peptides and immunomodulating compounds, useful for treatment of WT1-expressing cancers. This patent application covering WT1-targeting peptides linked to other molecules, which complements the Company’s existing composition of matter patents covering GPS peptides (which expire in 2033 not including any potential extensions), is expected to grant later this year, and will have a patent term that extends to at least 2026.
GFH009

On March 31, 2022, the Company and GenFleet, a clinical-stage biotechnology company developing cutting-edge therapeutics in oncology and immunology, announced that the companies entered into an exclusive license agreement that grants rights to SELLAS for the development and commercialization of GFH009, a highly selective CDK9 inhibitor, across all therapeutic and diagnostic uses worldwide outside of Greater China (mainland China, Hong Kong, Macau and Taiwan).

GFH009 is currently in a Phase 1 clinical trial in China and the United States which is planned to enroll approximately 80 patients including an expansion part 2. The fourth of six doses is currently being studied in this dose-escalation study. To date, stable disease has been observed in three patients, and a bone marrow blast decreased from 40% to 20% was observed in one AML patient at the 9 mg dose level, which is the third of the six dose levels to be studied in the Phase 1 trial.

Following completion of the Phase 1 clinical trial and achievement of a maximum tolerated dose, SELLAS plans to commence a Phase 2 clinical trial of GFH009 in combination with venetoclax and azacitidine in AML patients with active disease, likely by the end of the second quarter of 2023. The Company also plans to commence a Phase 1/2 basket clinical trial of monotherapy GFH009 in pediatric soft tissue sarcomas, including Ewing’s sarcoma and rhabdomyosarcoma, in late 2022 or early 2023, which it expects to complete by the end of 2023. Positive results from this program could ultimately provide the basis for a rare pediatric disease priority voucher.
Nelipepimut-S (NPS)

Since 2018, based on promising data from a cohort of patients with triple negative breast cancer ("TNBC") from a Phase 2b investigator sponsored clinical trial of the combination of trastuzumab (Herceptin) plus NPS in HER2 low expressing breast cancer patients in the adjuvant setting, the Company has been seeking out-licensing opportunities for NPS focused on the future clinical development of NPS in TNBC. After extensive effort, the Company has concluded that continued efforts to outlicense NPS for further development for breast cancer alone are unlikely to result in a licensing transaction commensurate with the value of the asset which the Company believes is due to the changing market for breast cancer therapies, the scope, cost and timeline for a Phase 3 trial which would satisfy regulatory requirements for the TNBC indication and the failure, in 2016, by the Company’s predecessor, Galena, of the Phase 3 clinical trial of monotherapy NPS in breast cancer. The Company is continuing its out-licensing strategy focusing on the potential for NPS in other cancer indications.
Corporate Updates:

Underwritten Public Offering: On April 5, 2022, the Company closed an underwritten public offering of 4,629,630 shares of its common stock and accompanying warrants to purchase up to 4,629,630 shares of common stock at a combined public offering price of $5.40 per share and accompanying warrant providing gross proceeds to the Company of $25.0 million before deducting underwriting discounts and commissions and offering expenses. The warrants to purchase shares of common stock have an exercise price of $5.40 per share, are immediately exercisable and will expire five years from the date of issuance.

Cash Position: As of December 31, 2021, cash and cash equivalents totaled approximately $21.4 million.

Enhanced Leadership Team:

In March 2022, SELLAS appointed Robert Francomano as Chief Commercial Officer.

In January 2022, the Company promoted John Burns to Senior Vice President, Finance, and Chief Accounting Officer.

In the fourth quarter of 2021 and the first quarter of 2022, the Company added heads of manufacturing and quality control/quality assurance functions.

Settlement of Legacy Galena Litigations:

In February 2022, SELLAS received the final court approval of the settlement of securities litigation relating to the Company’s predecessor, Galena, marking the end to all litigation related to activities of Galena. In November 2021, SELLAS received final court approval of the settlement of three derivative suits relating to the securities litigation.
Webcast Information

The Company will host a shareholder update call tomorrow morning, Wednesday, April 6, 2022, at 8:30 a.m. eastern time featuring remarks by Angelos M. Stergiou, MD, ScD. h.c., President and Chief Executive Officer of SELLAS.

To attend the live video webcast, please register or email KCSA Strategic Communications at [email protected].