On April 15, 2021 Affimed N.V. (Nasdaq: AFMD), a clinical-stage immuno-oncology company committed to giving patients back their innate ability to fight cancer, reported financial results for the year ended December 31, 2020 and provided an update on clinical and corporate progress (Press release, Affimed, APR 15, 2021, View Source [SID1234578090]).

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"2020 was an important year for Affimed. We continued to build on the strong foundation of our scientific discoveries and made significant progress across all our programs. We broadened our clinical pipeline, added new collaborations, built a strong balance sheet, appointed key senior management executives and ensured that our programs stayed on track through the global pandemic," said Dr. Adi Hoess, CEO of Affimed. "We entered 2021 with strong momentum, and the recently announced positive outcome of our interim futility analysis for our registration directed study of AFM13 as monotherapy in PTCL patients, and initial data from the trial investigating AFM13 pre-complexed natural killer cells in Hodgkin lymphoma patients provide further validation for our three-pronged development strategy. As we look ahead into 2021, we anticipate numerous additional updates as we advance our programs."

Clinical Stage Program Updates
Three-pronged Development Strategy

Based on preclinical and clinical data, Affimed is pursuing development of its innate cell engagers (ICE) as monotherapy, and in combination with adoptive NK cell transfer and PD-1/PD-L1 checkpoint inhibitors.

AFM13 (CD30/CD16A)

In March 2021, Affimed reported positive results from the preplanned interim futility analysis for AFM13-202, its phase 2 registration-directed study of AFM13 (CD16A/CD30) as monotherapy in patients with relapsed or refractory CD30-positive peripheral T-cell lymphoma (PTCL). The futility analysis demonstrated that the response rate in Cohort A achieved the predefined threshold for continuation of the study. The response rate in Cohort B was sufficiently comparable to allow merging of both cohorts into a single cohort for all patients with CD30 >1%, per the study protocol. Evidence of anti-tumor response was observed in both cohorts with complete and partial responses. The trial will continue by combining the high- and low-CD30 expressing cohorts into one.
In April 2021, Affimed reported positive initial clinical data from the investigator sponsored trial (IST) at The University of Texas MD Anderson Cancer Center evaluating increasing doses of cord-blood derived NK cells pre-complexed with AFM13 (CD16A/CD30) followed by three weekly infusions of AFM13 monotherapy in patients with recurrent or refractory CD30 positive lymphomas. As of March 31, 2021, all four response evaluable patients, including three patients in cohort 1 (1×106 AFM13-cbNK/kg) and one patient in cohort 2 (1×107 AFM13-cbNK/kg), have achieved an objective response, including two complete responses, according to investigator assessments by Lymphoma Response to Immunomodulatory Therapy Criteria (LYRIC). All four patients had relapsed / refractory Hodgkin lymphoma and were heavily pretreated, with between four and 14 previous lines of therapy which in all cases included brentuximab vedotin (Adcetris) and anti-PD1 antibodies.
AFM24 (EGFR/CD16A)

AFM24-101, the phase 1/2a clinical trial of AFM24, the EGFR/CD16A targeted ICE for patients with EGFR-expressing solid tumors, completed dose cohort 4 (160 mg) and patients are currently being enrolled and treated in dose cohort 5 (320 mg). Affimed expects to provide an update on the dose escalation and initiate the dose expansion cohorts during 2021.
An investigational new drug (IND) application was cleared by the U.S. Food and Drug Administration to investigate the combination of AFM24 with NKGen Biotech’s (formerly known as NKMax America) autologous NK cell therapy, SNK01, in a first-in-human proof of concept (POC) trial in patients with EGFR-expressing tumors. Affimed expects to initiate the study in the second half of 2021.
Affimed entered into a clinical collaboration with Roche for a phase 1/2a study evaluating AFM24 in combination with the PD-L1 checkpoint inhibitor atezolizumab (Tecentriq) in EGFR-expressing solid tumors. The phase 1 portion of the study will establish a dosing regimen and assess safety for the combination; in the subsequent phase 2a portion of the study, the clinical activity of the combination will be evaluated in specific tumor types. Affimed expects to initiate the study in the second half of 2021.
Preclinical data was presented at AACR (Free AACR Whitepaper) 2021 showing the potential of AFM24 as monotherapy and in combination with NK cells. As monotherapy, AFM24 induces tumor cell killing independent of KRAS mutations; and, in combination with adoptive NK cells, it leads to AFM24 dose-dependent tumor regression.
Preclinical and Partnered Programs
AFM28 progressed further in IND-enabling studies and Affimed expects an IND application will be filed in the first half of 2022.
In November 2020, Affimed entered into a licensing and strategic collaboration agreement with Roivant Sciences and granted Roivant a license to AFM32 with options for additional ICE molecules against targets not included in Affimed’s current pipeline. AFM32 will be investigated in solid tumors.
In August 2020, Affimed announced that Genentech’s RO7297089, a CD16A/BCMA targeting ICE, is actively recruiting patients into a first-in-human phase 1 trial resulting in the achievement of a milestone payment under the terms of the collaboration.
Affimed entered a collaboration with Artiva Biotherapeutics to assess feasibility and activity of pre-manufactured, co-vialed, cryopreserved, off-the-shelf NK cell combination therapeutics. The R&D collaboration is assessing the feasibility and preclinical activity of combinations of Artiva’s allogeneic NK cell product AB-101 and Affimed’s ICE molecules, building on earlier preclinical studies demonstrating synergistic cytotoxic activity.
Other Corporate Updates
In January 2021, Affimed completed a $115 million underwritten public offering to accelerate and expand the development and manufacturing of its clinical and preclinical ICE molecules.
In January 2021, Affimed entered into a financing agreement with Silicon Valley Bank for up to €25 million in term loans, with €10 million available at closing.
Full Year 2020 Financial Highlights
As of December 31, 2020, cash, cash equivalents and current financial assets totaled €146.9 million compared to €104.1 million on December 31, 2019. The pro forma cash position as of December 31, 2020, including net proceeds from the January 2021 underwritten public offering and the first tranche of the Silicon Valley Bank loan, would be approximately €244.5 million.
Based on its current operating plan and assumptions, Affimed anticipates that its cash and cash equivalents will support operations into the second half of 2023.
Net cash used in operating activities for the year ended December 31, 2020 amounted to €19.4 million compared to €29.1 million for the year ended December 31, 2019. The amount received in 2020 includes an initial upfront payment and committed funding of €33.3 million (US$ 40 million) from the Roivant collaboration.
Total revenue for the year ended December 31, 2020 was €28.4 million compared with €21.4 million for the year ended December 31, 2019. Revenue for 2020 and 2019 predominantly relate to the Genentech collaboration. Collaboration revenue for the year ended December 31, 2020 amounted to €27.8 million, with €26.2 million from the Genentech collaboration and €1.4 million from the Roivant collaboration. Collaboration revenue of €19.7 million for the year ended December 31, 2019 was from the Genentech collaboration.
Research and development expenses for 2020 increased 14.2% from €43.8 million in the year ended December 31, 2019 to €50.0 million in the year ended December 31, 2020, due to higher expenses for AFM24 and our other projects and infrastructure investments.
General and administrative expenses increased 33.6% from €10.3 million in the year ended December 31, 2019 to €13.7 million in the year ended December 31, 2020. In 2020, general and administrative expenses were largely comprised of personnel expenses of €6.3 million and legal, consulting and audit costs of €5.6 million.
Finance costs for the year ended December 31, 2020 were €6.6 million, compared to finance income of €15 thousand for the year ended December 31, 2019. Finance costs for the year ended December 31, 2020 were largely comprised of foreign exchange losses related to assets denominated in U.S. dollars as a result of the weakening of the U.S. dollar compared to the Euro during the year.
Net loss for the year ended December 31, 2020 was €41.4 million, or €0.50 per common share compared with a net loss of €32.4 million, or €0.50 per common share, for the year ended December 31, 2019. The weighted number of common shares outstanding for the year ended December 31, 2020 was 83.5 million.
Additional information regarding these results is included in the notes to the consolidated financial statements as of December 31, 2020 and "Item 5. Operating and Financial Review and Prospects," which will be included in Affimed’s Annual Report on Form 20-F as filed with the U.S. Securities and Exchange Commission (SEC).

Note on International Financial Reporting Standards (IFRS)
Affimed prepares and reports consolidated financial statements and financial information in accordance with IFRS as issued by the International Accounting Standards Board. None of the financial statements were prepared in accordance with Generally Accepted Accounting Principles in the United States. Affimed maintains its books and records in Euro.

Conference Call and Webcast Information
Affimed will host a conference call and webcast today, April 15, 2021 at 8:30 a.m. EDT to discuss fourth quarter 2020 financial results and recent corporate developments. The conference call will be available via phone and webcast.
To access the call, please dial +1 (646) 741-3167 for U.S. callers, or +44 (0) 2071 928338 for international callers, and reference passcode 4271307 approximately 15 minutes prior to the call.
A live audio webcast of the conference call will be available in the "Webcasts" section on the "Investors" page of the Affimed website at View Source A replay of the webcast will be accessible at the same link for 30 days following the call.

On April 15, 2021 CureVac N.V. (Nasdaq: CVAC), a global biopharmaceutical company developing a new class of transformative medicines based on messenger ribonucleic acid ("mRNA"), reported business updates and financial results for the fourth quarter and full-year 2020 (Press release, CureVac, APR 15, 2021, View Source [SID1234578088]).

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"2020 was a year of fundamental corporate transformation, which has propelled CureVac forward in its growth from a research-oriented biotech to an integrated, commercial biopharma company based on our unique mRNA technology and a broad clinical COVID-19 vaccine program," said Franz-Werner Haas, Chief Executive Officer of CureVac. "mRNA has emerged as a key technology that leads the charge against the COVID-19 pandemic, but it is only starting to realize its full potential in the development of new prophylactic vaccines and therapeutics in other areas such as oncology. Moving into 2021, we will continue the development of our company and, subject to regulatory approval, execute on our core mandate to broadly deliver a safe and effective COVID-19 vaccine. We have made great progress in achieving these goals and are now leveraging the solid foundation we laid to further tackle emerging variants in our COVID-19 vaccine program, advance into second-generation COVID-19 vaccines and infectious diseases and expand our clinical pipeline in oncology and protein therapies."

"We closed 2020 with a strong cash position of €1.32 billion, including the proceeds of a private round financing in July, our IPO in August and a grant from the German government in September. This was further complemented by a significant upfront payment from our Advanced Purchase Agreement with the European Commission for 225 million doses of CVnCoV with an option for an additional 180 million doses," said Pierre Kemula, Chief Financial Officer of CureVac. "In addition, in February 2021, we successfully raised aggregated gross proceeds of approximately $517.5 million in our first follow-on financing. With our strong cash position, we believe we are in a great position to accelerate our corporate transformation from a research-oriented biotech to a commercial-stage biopharma company and to continue to grow the business around our broad clinical pipeline while building up commercial expertise and infrastructure."

Selected Business Updates

Prophylactic Vaccines

CVnCoV – COVID-19 Vaccine Candidate

CVnCoV is CureVac’s first-generation vaccine candidate in its clinical COVID-19 vaccine program. Based on optimized, non-chemically modified mRNA, CVnCoV has shown to be well tolerated and to induce robust immune responses at a 12µg dose. CureVac’s technology enables CVnCoV to remain stable at standard refrigerator temperature for at least three months – a critical advantage as the world faces a pandemic that demands safe vaccines produced and distributed on a global scale.

Pivotal Phase 2b/3 in Europe and Latin America

The pivotal Phase 2b/3 study (HERALD), initiated on December 14, 2020, has successfully completed recruitment, with currently over 40,000 participants. Of those participants, approximately 75% were enrolled in Latin America and 25% were enrolled in Europe. The initial Phase 2b component of the study, assessing safety, reactogenicity and immunogenicity in study participants stratified according to age (18-60 and >60 years old), was completed in February 2021. Subsequently, the study advanced into the current Phase 3 safety and efficacy component.

The rapid spread of new virus variants across the world has supported the need to identify variants causing COVID-19 infections in the countries where the study is conducted for the case-driven interim analysis anticipated in the second quarter of 2021 as well as for all later trial analyses. According to variant surveillance sources (e.g. nextstrain.org), Variants of Concern, such as B.1.1.7 (UK strain), B.1.351 (South Africa strain) and P.1 (Brazil strain) currently constitute more than 50% of COVID-19 cases in Latin America and more than 80% in Europe. The highest prevalence is attributable to B.1.1.7. On March 30, CureVac submitted a trial protocol amendment to the regulatory authorities to address presently circulating virus variants via the implementation of a corresponding secondary endpoint.

Phase 2a in Peru and Panama

Our clinical Phase 2a, which served as a dose-confirmation trial following the selection of a 12µg dose for advanced clinical testing, has completed recruitment with 674 participants. Based on the high prevalence of COVID-19 in both countries since trial initiation, a relevant number of COVID-19 infections were detected within the still blinded trial. To harness the potential of this prevalence, CureVac submitted a protocol amendment to include a secondary endpoint for vaccine efficacy on March 31, 2021. The trial analysis is expected to allow collection of relevant efficacy data in the total population of the trial with a focus on the important sub-group of approximately 270 participants above the age of 60, who received 12µg of CVnCoV, thereby complementing Phase 2b/3 efficacy data.

First Preclinical Challenge Study on Variant of Concern B.1.351 (South Africa Variant)

On March 23, CureVac published the first challenge infection study in a preclinical mouse model to show protection against a SARS-CoV-2 Variant of Concern. The data demonstrate the protection efficiency of CVnCoV from the SARS-CoV-2 original strain, BavPat1, and the novel Variant of Concern, B.1.351 (South African variant), in a transgenic mouse model. CVnCoV has shown to fully protect mice from lethal infection caused by BavPat1 or B.1.351. Immunization resulted in the induction of RBD binding and virus-neutralizing antibodies and conferred complete and robust protection from viral replication in the lung and the brain. In this model, very limited viral replication was observed in the upper respiratory tract of mRNA-vaccinated animals challenged with B.1.351.

The study expands the data basis of existing preclinical studies of CVnCoV by providing relevant SARS-CoV-2 variant-specific data and adds further evidence on the overall protection efficiency of CVnCoV. Detailed data can be accessed through a manuscript available on the bioRxiv pre-print server.

Expansion of the Clinical COVID-19 Vaccine Program

CureVac is continuously expanding the COVID-19 vaccine program to generate important clinical data on CVnCoV to better serve differentiated protection needs during the pandemic.

On March 27, a protocol amendment was filed for the ongoing Phase 2a study in Peru and Panama to enroll approximately 40 adolescent participants between the ages of 12 and 17. Enrollment of the first participants is expected to start toward the end of April and it forms the first part of a broader study in this age group. Contingent on a successful safety review, the study is planned to recruit a larger number of adolescent participants and allow for geographical reach into other Latin American countries and Europe.

An additional Phase 3 trial, to evaluate the safety, reactogenicity and immunogenicity of CVnCoV in adults with an elevated risk of severe COVID-19 infection due to comorbidities is expected to start shortly. Selected comorbidities include obesity, chronic cardio­vascular disease, chronic kidney disease, chronic obstructive pulmonary disease (COPD), HIV, type 2 diabetes mellitus and post-renal transplantation. The multicenter clinical trial will be conducted in Belgium and is expected to enroll approximately 1,200 participants.

In early May, CureVac together with its partner Bayer plans to initiate a flu-co-administration study to assess compatibility with established seasonal vaccines in case of seasonal COVID-19 vaccinations. The Phase 3 multicenter study will evaluate the safety, reactogenicity and immuno­genicity of CVnCoV co-administered with a licensed quadrivalent influenza vaccine in adults 60 years and older. The co-administration will be tested versus the separate administration of both vaccines. The study aims to enroll approximately 1,000 participants.

Further age-related data is expected to be generated in an upcoming Phase 2 trial, focusing on immuno­genicity, including a deep characterization of the immune response in older adults above the age of 65 compared to younger adults aged 18-45. With a focus on sophisticated immunogenicity markers, the non-randomized, open-label clinical trial is expected to start in the second quarter. It will be conducted in France and aims to include approximately 180 participants.

Regulatory Pathway

To expedite the route to potential market authorization of CVnCoV, CureVac initiated a rolling submission with the European Medicines Agency (EMA) on February 12, 2021. The process was started with the submission of a first preclinical data package and was recently advanced with two additional data packages, including CMC data as well as first clinical data from CureVac’s dose-escalation Phase 1 trial. CureVac currently anticipates completing data submission in time to file for conditional approval of CVnCoV in Q2 2021.

Executing on Advancing a Commercial Infrastructure

As a part of the corporate transformation, CureVac is developing its commercial organization and has started the preparation of commercial territories for the anticipated launch of CVnCoV and future products. A commercial infrastructure is rapidly growing under the leadership of Dr. Antony Blanc, appointed as Chief Business and Chief Commercial Officer in December 2020. In March 2021, CureVac established a legal entity in Switzerland, which represents a first step in preparing access to commercial territories outside the European Union. Next to Germany and Austria, Switzerland represents one of the three countries for which CureVac holds exclusive commercialization rights for Program Products in the context of CureVac’s broad GSK partnership in vaccines for infectious diseases as well as second-generation vaccines for COVID-19.

Manufacturing of COVID-19 vaccine candidate, CVnCoV

As announced on November 17, 2020, CureVac is ramping up its broad and integrated European vaccine-manufacturing network with highly experienced Contract Development and Manufacturing Organization (CDMO) partners and the additional support of its strategic partners Bayer and GSK. The network is supported by CureVac’s in-house GMP III manufacturing suite – the blueprint for the optimized production processes for CVnCoV established in 2020. Since initiation, several partners have joined the network, covering the main manufacturing steps for CVnCoV, thereby expected to mitigate supply chain risks and increase manufacturing flexibility. Manufacturing experts, such as Wacker Chemie, Fareva, Rentschler Biopharma, Novartis, and most recently Celonic Group, make up most of the network of CDMO partners. The network is expected to expand throughout 2021 to provide an anticipated manufacturing capacity of up to 300 million doses. For 2022, CureVac raised its capacity guidance from up to 600 million to up to 1 billion doses.

In-house manufacturing capacity is expected to further expand when GMP IV, CureVac’s large-scale production facility supported by the European Investment Bank, comes online. This new facility is anticipated to open in the second half of 2022.

In 2020, CureVac also advanced the RNA Printer, a novel downsized, mobile and automated GMP production system for downscaled manufacturing of mRNA therapeutics. With its modular design and decentralized concept, the RNA Printer is particularly well suited for pandemic preparedness in outbreak scenarios or as a stand-alone device in front lines of epidemic areas.

Partnership Agreements

CureVac recently entered into three strategic COVID-19 collaborations, with highly experienced pharma and science partners, to accelerate the continued development of a broad pipeline of first and second-generation COVID-19 vaccines. Together with its partners, CureVac aims to provide a robust solution for the pandemic and the rapid spread of new variants based on its first-generation COVID-19 lead vaccine candidate, CVnCoV, as well as advanced next-generation vaccines to create value also beyond the COVID-19 pandemic.

To expedite market readiness of CVnCoV, CureVac and Bayer announced a collaboration and service agreement on January 7, 2021, under which Bayer will contribute expertise, infrastructure and workforce to support CVnCoV in areas such as clinical operations, regulatory affairs, pharmaco­vigilance, medical affairs and supply chain performance as well as operational support in selected countries.

On February 3, 2021, CureVac and GSK announced the extension of their July 2020 strategic technology collaboration in infectious diseases to jointly develop second-generation COVID-19 vaccines based on new mRNA backbones in single and multivalent formats.

As a targeted approach to rapidly spreading Variants of Concern, both collaborations will be complemented by the scientific expertise provided via CureVac’s R&D collaboration with the UK Government and its Vaccines Task Force. The collaboration, announced on February 5, 2021, and currently in final negotiation stage is designed to fast-track the development and regulatory pathway of variant-optimized vaccines based on the Vaccine Task Force’s renowned expertise in variant epidemiology and genomics.

Oncology

CV8102 – Cancer immuno-modulator in solid tumors

Phase 1

CureVac’s lead oncology candidate, CV8102, is being assessed in a Phase 1 dose-escalation study, evaluating tolerability and activity in the dose range of 25µg to 900µg as a single agent and in combination with systemic anti-PD-1 antibodies. Intra-­tumoral treatment tested in four types of solid tumors (cutaneous melanoma, adenoid cystic carcinoma, squamous cell carcinoma of skin and squamous cell carcinoma of head and neck) had formerly shown objective tumor responses in two melanoma patients and two additional patients with stable disease, including shrinkage of non-injected lesions in the single-agent cohort. At the Society for Immunotherapy of Cancer (SITC) (Free SITC Whitepaper) conference on November 9, 2020, CureVac reported that these findings were further extended by a new partial response observed in a patient with cutaneous squamous cell carcinoma who was pre-treated with anti-PD-1, expanding activity from melanoma into a second indication. Additionally, the first RECIST response in the PD-1 combination cohort was observed in a PD-1 refractory melanoma patient with regression of non-injected lesions in the lung and liver.

Based on the results, on February 4, 2021, CureVac announced the expansion of the Phase 1 study to confirm the safety, tolerability and efficacy of CV8102 at a 600μg dose, selected to be advanced in a Phase 2 clinical trial. The expansion part of the Phase 1 trial will enroll 30 patients with PD-1 refractory melanoma who will receive intra-tumoral injections of CV8102 in combination with PD-1 antibodies as well as 10 patients who will be treated with CV8102 only.

Financial Update for the Fourth Quarter and Full-Year of 2020

Cash Position

Cash increased from €30.7 million as of December 31, 2019, to €1,322.6 million as of December 31, 2020, mainly due to the €559.3 million raised in the 2020 Private Investment in July 2020, along with €192.9 million in proceeds, net of underwriting discounts and commission, from CureVac’s initial public offering (IPO) on the Nasdaq in August 2020 and a €120 million non-refundable upfront payment received from GSK. The Company also received €103 million in payments from the grant provided by the German Federal Ministry of Education and Research (BMBF) in the fourth quarter of 2020. The total amount of the grant is €252 million; therefore, provided we fulfill the grant conditions, we are entitled for further €149 million in 2021. In addition, the Company collected an up-front payment of €450 million paid by the European Commission on behalf of the Member States in December 2020. Cash used in the operations in the year was mainly used to advance all R&D activities for CVnCoV, our COVID-19 vaccine candidate, during the second half of Fiscal Year 2020.

Revenues

Revenue was €6.0 million and €48.9 million for the three and twelve months ended December 31, 2020, respectively, representing a decrease of €0.8 million for the three months and an increase of €31.5 million, or -11.8% and +181.0%, from €6.8 million and €17.4 million for the same periods in 2019, respectively.

These increases were primarily driven by the following events: in July 2020, GlaxoSmithKline plc (GSK) and CureVac signed a strategic collaboration agreement for the research, development, manufacturing and commercialization of mRNA-based vaccines and monoclonal antibodies targeting infectious disease pathogens. In addition to an equity investment of €150 million, made as part of the 2020 Private Investment, GSK made a non-refundable upfront payment of €120 million, which has been deferred and recognized as a contract liability. For the three months ended December 31, 2020, €4.1 million was released from contract liabilities and recognized as revenues. In June 2020, CureVac and Eli Lilly terminated their collaboration. As a result, on the termination date, €33.1 million in contract liabilities from an upfront payment was recognized as revenue as no further associated performance obligations remained.

Operating result

Operating loss was €46.6 million and €109.8 million for the three and twelve months ended December 31, 2020, respectively, representing an increase of €11.5 million and €10.3 million, or an increase of
32.8% and 10.4%, from €35.1 million and €99.5 million for the same periods in 2019, respectively. The increase in operating loss in the three months ended December 31, 2020 was mainly driven by higher research and development costs, primarily due to high costs for CVnCoV R&D activities, including research material manufacturing expenses. The increase was partially offset by other operating income driven by higher cost reimbursements received from the Coalition for Epidemic Preparedness Innovations (CEPI) and the German Federal Ministry of Education and Research (BMBF). For the twelve months ended December 31, 2020, the increased operating loss was mainly driven by higher research and development costs, primarily due to high costs for CVnCoV R&D activities, including research material manufacturing expenses, which began in 2020. This was partially offset by recognition of the €33.1 million in contract liabilities upon termination of the Eli Lilly collaboration. In addition, the increase in R&D costs was partially offset by a decrease in cost of sales during both of these periods in 2020 as compared to 2019 due to lower set-up activities and lower product manufacturing for our collaboration partners.

Financial Result

Financial result was €-10.7 million and €-20.0 million for the three and twelve months ended December 31, 2020, respectively, representing a decrease of €-9.9 million and €-19.4 million from €-0.8 million and €-0.6 million for the same period in 2019, respectively. Financial result for the twelve months ended December 31, 2020, contains mainly interest for the convertible loans, which were fully repaid, including interest, in August 2020, negative interests on cash which is being held in liquid funds for use in our CVnCoV R&D and manufacturing activities and a negative impact of the FX mainly in the fourth quarter of the year.

Earnings before Taxes (EBT)

Earnings before Taxes (EBT) was €-57.3 million and €-129.8 million for three and twelve months ended December 31, 2020, compared to Earnings before Taxes of €-35.9 million and €-100.1 million in the same respective periods of 2019.

Conference Call and Webcast

CureVac will host an analyst and investor webcast and conference call on Thursday, April 15, 2021 at 4:00 p.m. CET / 10:00 a.m. EST. The live conference call dial-in details and webcast link can be accessed via the Investor Relations section of the CureVac homepage at View Source

Corresponding presentation slides will be posted shortly before the start of the webcast. A replay will be made available at this website after the event.

On April 15, 2021 OncoSec Medical Incorporated (NASDAQ:ONCS) (the "Company" or "OncoSec"), a biotechnology company focused on cytokine-based intratumoral immunotherapies, reported that it will be presenting encore interim data from its KEYNOTE-695 registration-enabled Phase 2b clinical trial evaluating TAVO (tavokinogene telseplasmid), a DNA plasmid-based interleukin-12 (IL-12), in combination with KEYTRUDA (pembrolizumab) in rigorously defined anti-PD1 checkpoint resistant metastatic melanoma patients at the 10th World Congress of Melanoma (Press release, OncoSec Medical, APR 15, 2021, View Source [SID1234578087]). This is an encore presentation of data presented at The Society for Immunotherapy of Cancer (SITC) (Free SITC Whitepaper)’s (SITC) (Free SITC Whitepaper) 2020 Annual Meeting. Presenters will also discuss the therapeutic potential of OncoSec’s DNA medicines platform to elicit robust anti-tumor immunity via intratumoral gene electrotransfer of TAVO plus CXCL9.

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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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"Achieving an overall response rate of 30% with several complete responses and no serious adverse events is extremely encouraging for checkpoint resistant metastatic melanoma patients who currently rely on systemic administration of immune-stimulating drugs associated with severe toxicity," said Paolo A. Ascierto, M.D., Director of the Unit of Melanoma, Cancer Immunotherapy and Innovative Therapy at the National Tumor Institute Fondazione G. Pascale in Naples, Italy. "The data reported, in addition to its ease of use, demonstrate the potential of TAVO in combination with pembrolizumab as a next-generation intratumoral IL-12 therapy that can induce regression of both locally treated and untreated distant and visceral lesions."

OncoSec’s presentation is summarized below:

Introduction
Presenter: Christopher G. Twitty, Ph.D.
Session Date/Time: Saturday, April 17, 2021, 4:15 p.m. – 4:18 p.m. ET

OncoSec’s KEYNOTE-695 interim data
Presenter: Paolo Ascierto, M.D.
Session Date/Time: Saturday, April 17, 2021, 4:18 p.m. – 4:28 p.m. ET

OncoSec’s next generation therapies: amplification of the CRX3/CXCL9 axis via intratumoral electroporation of CXCL9 synergizes with IL-12 therapy (TAVO) to elicit robust anti-tumor immunity
Presenter: Christopher G. Twitty, Ph.D.
Session Date/Time: Saturday, April 17, 2021, 4:28 p.m. – 4:48 p.m. ET

Live Q&A
Presenters: Christopher G. Twitty, Ph.D., Paolo Ascierto, M.D.
Session Date/Time: Saturday, April 17, 4:48 p.m. – 5:15 p.m. ET

The conference will be held virtually from April 15 – 17, 2021. To access the conference virtual platform, visit: View Source

About KEYNOTE-695
KEYNOTE-695 is OncoSec’s registration-directed Phase 2b trial (NCT#03132675) evaluating TAVO (tavokinogene telseplasmid), a DNA plasmid-based interleukin-12 (IL-12) + KEYTRUDA (pembrolizumab) in patients with rigorously confirmed anti-PD-1 checkpoint resistant metastatic melanoma. The trial aims to enroll up to 100 patients with refractory, locally advanced or metastatic disease defined as unresectable Stage III/IV metastatic melanoma that had definitively progressed on a full-course of anti-PD-1 treatment with KEYTRUDA (pembrolizumab) or OPDIVO (nivolumab). TAVO has received Fast Track Designation from the U.S. Food and Drug Administration (FDA) for the treatment of metastatic melanoma following progression on KEYTRUDA or OPDIVO.

About TAVO
OncoSec’s gene therapy technology combines TAVO (tavokinogene telseplasmid), a DNA plasmid-based interleukin-12 (IL-12), with an intra-tumoral electroporation gene delivery platform to achieve endogenous IL-12 production in the tumor microenvironment that enables the immune system to target and attack tumors throughout the body. TAVO has demonstrated a local and systemic anti-tumor response in several clinical trials, including the pivotal Phase 2b trial KEYNOTE-695 for metastatic melanoma and the KEYNOTE-890 Phase 2 trial in triple negative breast cancer (TNBC). TAVO has received both Orphan Drug and Fast-Track Designation by the U.S. Food & Drug Administration for the treatment of metastatic melanoma.

On April 15, 2021 Kaleido Biosciences, Inc. (Nasdaq: KLDO), a clinical-stage healthcare company with a differentiated, chemistry-driven approach to targeting the microbiome to treat disease and improve human health, reported that CEO Dan Menichella will participate in an analyst-led fireside chat on Thursday, April 22 at the Jefferies Microbiome-Based Therapeutics Summit (Press release, Kaleido Biosciences, APR 15, 2021, View Source [SID1234578086]).

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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

                  Schedule Your 30 min Free Demo!

The webcast of the fireside chat will be made available that morning as of 8am EDT on the Investors & Media section of Kaleido’s website at View Source An archived replay will be available for 90 days following the event.

On April 15, 2021 Invitae Corporation (NYSE: NVTA), a leading medical genetics company, reported research showing one in six people with colorectal cancer harbor genetic changes that are known to substantially increase the risk for cancer, especially in patients who were younger when diagnosed (Press release, Invitae, APR 15, 2021, View Source [SID1234578085]). The findings are the latest from a landmark study of genetic testing across many solid tumor cancers and were presented at the 2021 American College of Medical Genetics and Genomics (ACMG) Annual Clinical Genetics Meeting.

Schedule your 30 min Free 1stOncology Demo!
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

                  Schedule Your 30 min Free Demo!

Invitae’s (NVTA) mission is to bring comprehensive genetic information into mainstream medical practice to improve the quality of healthcare for billions of people. www.invitae.com (PRNewsFoto/Invitae Corporation)

"Colorectal cancer is one of the most common types of cancer. Recently we’ve seen an unfortunate increase in incidence among people younger than 50 years old. Improving our understanding of who is at risk and implementing appropriate screening strategies is essential to ensuring these cancers are caught and treated earlier when outcomes are typically better," said Robert Nussbaum, M.D., chief medical officer of Invitae. "Access to information about inherited risk factors is also important after diagnosis, not only for the patients themselves in whom a change in treatment was made in more than 10 percent of patients based on genetic test results, but also in alerting other family members of the need to be tested to see if they are also at increased risk and need more intensive surveillance to catch cancer early and prevent more serious disease."

The study evaluated the utility of universal multigene panel testing and found the use of multigene panel testing in colorectal cancer was associated with an increased detection of heritable mutations over guideline-based testing. In the study, 361 colorectal cancer patients received germline genetic testing using a panel that included more than 80 genes linked to increased cancer risk. Cancer-linked genetic changes were found in 15.5% (n=56) of patients predominantly in moderate and high penetrance cancer susceptibility genes such as APC, BRCA2 and TP53. The median age of patients in the study was 57 years, 43.5% were female, 82% were white and 38.2% had stage IV disease.

Younger age at diagnosis was associated with a higher likelihood of finding genetic changes linked to increased cancer susceptibility. Research from the American Cancer Society has shown rates have been increasing since the mid-1980s in adults ages 20-39 years and since the mid-1990s in adults ages 40-54 years, with younger age groups experiencing the steepest increase.