Positive clinical results for TG4001 and TG6002 and financial visibility secured until 2022

• TG4001: Very promising results from Phase 1b/2 trial in HPV-positive cancers
• TG6002: Initial translational results confirm the value of intravenous administration
• Preclinical and clinical projects progressing despite the Covid-19 pandemic
• €33.2 million of cash at the end of June 2020 was followed by the receipt of €19 million due to the partial sale of the stake in Tasly BioPharmaceuticals in August 2020, providing financial visibility until 2022
• Succession of the Chairman and Chief Executive Officer planned at the end of 2020

 

 

Conference call scheduled today at 6:00 p.m. CET (in English). See details below.

 

 

Strasbourg, France, September 16, 2020, 5:45 p.m. CET – Transgene (Euronext Paris: TNG), a biotech company that designs and develops virus-based immunotherapies for the treatment of cancer, today publishes its financial results for the six-month period ended June 30, 2020, and provides an update on progress of its portfolio.

 

Philippe Archinard, Chairman and Chief Executive Officer of Transgene, commented:

“I would like to thank the teams at Transgene for their remarkable job in advancing all our clinical and preclinical projects in an environment that has been severely disrupted by the Covid-19 pandemic.

During the period we delivered positive Phase 1b/2 results with TG4001, which have given us the confidence to progress the clinical development of this therapeutic vaccine against HPV-induced cancers. We intend to provide more detail on these positive Phase 1b/2 study results in the coming months.

Our oncolytic virus TG6002 showed positive initial data in a Phase 1 trial, indicating that it induces the production of a chemotherapy agent in the tumor. These promising results confirm the safety of TG6002 when given intravenously and are highly supportive of the new generations of oncolytic viruses that we are developing based on our exciting Invir.IO™ platform.

Patient inclusion continues in line with expectations in the first trials of the individualized immunotherapy TG4050, which has been generated from our myvac® platform. The myvac® platform and the launch of these trials earlier this year exemplify our technological leadership in individualized immunotherapies. The data which were presented at the AACR congress in June highlighted the power of NEC’s artificial intelligence and the integration of the first block chain solution into the myvac® production process. In parallel, we successfully produced the first clinical batches of TG4050.

The collaboration with AstraZeneca continues with the delivery of new oncolytic viruses.

Finally, by selling part of approximately 40% of the stake in Tasly BioPharmaceuticals for $22.2 million, Transgene has the cash resources to fund its activities until 2022.”

Promising initial data for TG4001

 

The analysis of the efficacy data from the Phase 1b/2 trial combining TG4001 with avelumab in HPV16-positive recurrent and/or metastatic malignancies showed a promising clinical activity in the overall study population (34 evaluable patients).

 

In addition, Transgene identified a selection criterion corresponding to patients showing particularly encouraging clinical activity. For more than 50% of these patients, the disease had not progressed at 12 weeks, compared to an expected median progression-free survival (PFS) of 8 weeks for this population with current treatment regimens or with immune checkpoint inhibitors in monotherapy. Responses are durable in most of the responder patients. Transgene is currently completing translational analyses. Patient follow-up is still ongoing. Complete data will be presented at an upcoming scientific conference.

 

Transgene intends to pursue the development of TG4001 and is actively working on the preparation of a confirmatory clinical study.

 

Advanced technological leadership with the myvac® platform

 

Transgene is developing the therapeutic vaccine TG4050, together with NEC. This individualized cancer vaccine is based on the myvac® platform and integrates NEC’s artificial intelligence capabilities.

 

The first Phase 1 clinical trials assessing TG4050 in patients with ovarian and head and neck cancers started in January 2020 in Europe and in the United States. NEC is financing 50% of these studies.

 

The Company has set up an in-house production unit dedicated to the manufacturing of the individualized clinical batches of TG4050 needed for each patient. This unit is operational and complies with good manufacturing practice (GMP) norms. The manufacturing process and unit have been validated and the first clinical batches have been produced.

 

The myvac® platform is being actively promoted as it exemplifies Transgene’s technological leadership in individualized immunotherapies.

• Data validating the vaccine design principle and underlining the accuracy of the artificial intelligence used to personalize TG4050 were presented at the AACR congress (June 2020).
• Transgene has implemented the first block chain solution dedicated to the traceability of personalized treatment in clinical trials. This cloud-based solution monitors and orchestrates all of the processes related to the design and manufacturing of Transgene’s individualized therapeutic vaccine TG4050.
• Other innovative approaches were integrated into the myvac® approach and will be detailed in the coming months.

 

The initial translational data of TG6002 highlight the potential of the Invir.IO™ platform

 

Initial data from the Phase 1 trial confirm the good tolerability of TG6002 in humans and demonstrate that this Vaccinia Virus, which is the viral backbone on which the Invir.IO™ platform is based, can reach the tumor and replicate within these cancer cells when administered intravenously.

 

BT-001 is the first oncolytic virus from the Invir.IO™ platform. A first-in-human trial is being prepared; the trial protocol has been filed in France and in Belgium. Promising preclinical results for BT-001 were presented at the AACR annual congress (June 2020).

 

The collaboration with AstraZeneca continues with the development of new innovative oncolytic viruses. AstraZeneca can exercise an option to further develop each of these novel drug candidates.

Summary of key ongoing clinical trials

 

 

TG4001 + Bavencio® (avelumab) Phase 1b/2

Targets: HPV16 E6 and E7 oncoproteins Advanced HPV-positive cancers including oropharyngeal head and neck cancer – 2nd line ü Clinical collaboration with Merck KGaA and Pfizer, for the supply of avelumab ü Very promising results; patient follow-up is ongoing Ü Detailed results will be presented at an upcoming scientific conference Ü Transgene intends to launch a larger, controlled, confirmatory trial

 

 

myvac®       TG4050 Phase 1	Targets: tumor neoantigens ü Data demonstrating the high accuracy of AI-based neoantigen prediction technology used to design TG4050 were presented at AACR Ovarian cancer – after surgery and first-line chemotherapy ü Trial authorized in the United States and in France ü First patient enrolled in January 2020 – inclusions progressing in line with forecast Ü First scientific communication in 2021
TG4050 Phase 1	HPV-negative head and neck cancer – after surgery and adjuvant therapy ü Trial authorized in the United Kingdom and in France ü First patient enrolled in January 2020 – inclusions progressing in line with forecast Ü First scientific communication in 2021

 

 

TG6002 Phase 1/2a	Payload: FCU1 for the local production of a 5-FU chemotherapy Gastro-intestinal cancer (colorectal cancer for Phase 2) – Intravenous (IV) administration ü Multicenter trial ongoing in Belgium, France and Spain ü First findings confirm that 5-FU is produced in the tumor Ü Dose escalation is ongoing in the Phase 1 part, testing additional dose levels
TG6002 Phase 1/2a	Colorectal cancer with liver metastasis – Intrahepatic artery (IHA) administration ü Multicenter trial authorized in the United Kingdom ü First patient treated in February 2020; enrollment resuming in September 2020 after pausing due to Covid-19 Ü First observations in 2021

 

 

Invir.IO™ BT-001 Phase 1/2

Payload: anti-CTLA4 antibody and GM-CSF cytokine Solid tumors ü Collaboration with BioInvent ü First clinical trial applications submitted (France and Belgium) ü Presentation of very encouraging preclinical results at AACR 2020 Ü Approval from health authorities expected before the end of 2020

 

Key Financials

 

The Board of Directors of Transgene met on September 16, 2020 and approved the financial statements for the six-month period ended June 30, 2020. The Statutory Auditors have conducted a limited review of the interim consolidated financial statements.

 

The half-year financial report is available on Transgene’s website, https://www.transgene.fr.

 

Key elements of the income statement

 

(in thousands of euros)	June 30, 2020	June 30, 2019
Operating revenues	5,731	4,909
Research and development expenses	(13,831)	(14,668)
General and administrative expenses	(3,297)	(3,572)
Other expenses	-	(141)
Operating expenses	(17,128)	(18,381)
Operating income/(loss)	(11,397)	(13,472)
Financial income/(loss)	9,183	(1,870)
Net income/(loss)	(2,214)	(15,342)

 

Operating revenues amounted to €5.7 million for the first six months of 2020 compared to €4.9 million for the same period in 2019.

 

• In 2019, the Company entered into a collaboration agreement with AstraZeneca with exclusive licensing options to co-develop oncolytic immunotherapies derived from the Invir.IO™ platform. As a result, in the first half of 2019 Transgene received €8.9 million (US$10 million) in fees for access to its platform. This initial payment is recognized as revenue based on the stage of completion of the related activities. Over the period, the income recognized under this collaboration agreement was €2.2 million (€0.7 million in the first half of 2019). Of this amount €1.8 million reflects recognition of the initial payment for work done during the period and €0.4 million for the achievement of certain preclinical milestones.
• The research tax credit amounted to €2.9 million for the first half of 2020, compared to €3.1 million for the first half of 2019.

 

Research and Development (R&D) expenses amounted to €13.8 million in the first half of 2020 compared to €14.7 million for the same period in 2019. External expenses for clinical projects decreased to €3.0 million from €4.7 million in the first half of 2019. This decrease is mainly due to a reduction in subcontracted clinical batch production expenses in the first half of 2020 compared to the same period in 2019.

 

General and administrative expenses amounted to €3.3 million for the first half of 2020 compared to €3.6 million for the same period in 2019.

 

Net interest income amounted to a gain of €9.2 million in the first half of 2020 compared to an expense of €1.9 million for the same period in 2019. This change is mainly due to the increase in the fair value of Tasly Biopharmaceuticals shares: in July 2020, the sale of the shares was carried out at a higher price than the acquisition price in July 2018. This sale price was applied to all the shares held.

 

As a consequence, the net comprehensive loss amounted to €2.2 million for the first half of 2020 compared to a loss of €15.3 million for the same period in 2019.

 

As of June 30, 2020, the Company’s cash, cash equivalents and other financial assets amounted to €33.2 million versus €43.3 million as of December 31, 2019.

Transgene’s cash burn amounted to €10.1 million in the first half of 2020, compared with €4.1 million for the same period in 2019.

 

Transgene intends to reimburse the €10 million bank loan from the European Investment Bank in advance of its June 2021 maturity.

 

The Company confirms its financial visibility until 2022.

 

Partial sale of the stake in Tasly BioPharmaceuticals

 

On August 4, 2020, Transgene announced the receipt of $22.2 million (€19 million) following the sale to a Chinese investment fund of part of its minority stake in Tasly BioPharmaceuticals. This transaction involved the sale of 10.3 million shares of Tasly BioPharmaceuticals (38% of the shares held by Transgene).

Following this share sale, Transgene holds 17.1 million shares in Tasly BioPharmaceuticals, equivalent to 1.58% of the Chinese company’s capital. Transgene’s remaining shareholding in Tasly BioPharmaceuticals is valued at approximately $36.9 million based on the price of the current share sale.

At the end of August 2020, Tasly BioPharmaceuticals filed its IPO documentation with the Science and Technology Innovation Board (STIB) of the Shanghai Stock Exchange.

 

Succession of the Chairman and Chief Executive Officer planned at the end of 2020

 

Philippe Archinard, Chairman and Chief Executive Officer of Transgene, has informed the Board of Directors of his intention to leave his position at the end of 2020 to take up new responsibilities within Institut Mérieux. The Board has acknowledged his decision and proposes that his successor be Hedi Ben Brahim, who has been a Board member of Transgene since May 2019. This decision will be approved at the Board meeting scheduled on December 3, 2020. Philippe Archinard will remain a Board Member of Transgene thereafter. 

 

A conference call in English is scheduled today, on September 16^th, 2020, at 6:00 p.m. CET.

 

Webcast link to English language conference call:

https://channel.royalcast.com/webcast/transgene/20200916_1/

 

Participant telephone numbers:

France: +33 (0) 1 7037 7166 United Kingdom: +44 (0) 20 3003 2666 United States: +1 212 999 6659

Confirmation code: Transgene

 

A replay of the call will be available on the Transgene website (www.transgene.fr) following the live event.

 

Contacts

 

Transgene: Lucie Larguier Directeur Communication Corporate & Relations Investisseurs +33 (0)3 88 27 91 04 investorrelations@transgene.fr

Media: Citigate Dewe Rogerson David Dible/Sylvie Berrebi + 44 (0)20 7638 9571 transgene@citigatedewerogerson.com

 

About Transgene

Transgene (Euronext: TNG) is a publicly traded French biotechnology company focused on designing and developing targeted immunotherapies for the treatment of cancer. Transgene’s programs utilize viral vector technology with the goal of indirectly or directly killing cancer cells.

The Company’s clinical-stage programs consist of two therapeutic vaccines (TG4001 for the treatment of HPV-positive cancers, and TG4050, the first individualized therapeutic vaccine based on the myvac® platform) as well as two oncolytic viruses (TG6002 for the treatment of solid tumors, and BT-001, the first oncolytic virus based on the Invir.IO™ platform).

With Transgene’s myvac® platform, therapeutic vaccination enters the field of precision medicine with a novel immunotherapy that is fully tailored to each individual. The myvac® approach allows the generation of a virus-based immunotherapy that encodes patient-specific mutations identified and selected by Artificial Intelligence capabilities provided by its partner NEC.

With its proprietary platform Invir.IO™, Transgene is building on its viral vector engineering expertise to design a new generation of multifunctional oncolytic viruses. Transgene has an ongoing Invir.IO™ collaboration with AstraZeneca. 

Additional information about Transgene is available at: www.transgene.fr.

Follow us on Twitter: @TransgeneSA