HOOKIPA Phase 1 HB-200 data show unprecedented T cell response, favorable tolerability, and preliminary efficacy as monotherapy for advanced HPV16+ cancers

On June 7, 2021 HOOKIPA Pharma Inc. (NASDAQ: HOOK, ‘HOOKIPA’), a company developing a new class of immunotherapeutics based on its proprietary arenavirus platform, reported positive Phase 1 data from its ongoing Phase 1/2 study (NCT04180215) of HB-200 for the treatment of advanced Human Papillomavirus 16-positive (HPV16+) cancers (Press release, Hookipa Biotech, JUN 7, 2021, View Source [SID1234583652]). Data presented as an oral presentation (abstract #2502) at the 2021 American Society of Clinical Oncology (ASCO) (Free ASCO Whitepaper) Annual Meeting showed outstanding T cell responses, preliminary efficacy as a monotherapy in heavily pretreated patients who progressed on standard of care, including checkpoint inhibitors, and favorable tolerability. The company also announced translational data suggesting a relationship between T cell response and potential clinical efficacy. The company will host an investor event today at 6:30pm EDT.

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"Our early Phase 1 HB-200 data provide compelling clinical evidence of the potential of our versatile arenaviral platform to introduce a new class of immunotherapeutics that can generate an unprecedented T cell response to the desired cancer target," said Joern Aldag, Chief Executive Officer at HOOKIPA. "We’re in dose escalation phase in a group of heavily pre-treated HPV16+ cancer patients, so we’re thrilled to see response rates with HB-201 monotherapy in head and neck cancer patients that one would expect only in earlier lines of therapy. Moreover, initial clinical biopsy data validate the proof of mechanism, highlighting the potential for our technology to address unmet needs across various cancers. We’re excited to share further data as the HPV16+ cancer trial continues, and we look forward to initiating registration-enabling studies in early 2022."

Up to the March 31 cut-off date, 38 patients with metastatic HPV16+ tumors had received HB-200 therapy: 14 received HB-201 intravenously every three weeks, 8 received alternating HB-201/HB-202 intravenously every three weeks, and 16 received other regimens. Most of the patients (32) have squamous cell head and neck tumors; patients with other tumor types included three with cervical, one with vaginal, one with anal, and one with penile. Participants received a median of three prior therapies (ranging from one to 10), and 82 percent (31 participants) had progressed on a checkpoint inhibitor regimen. Seventy-nine percent had baseline distant metastasis, underscoring the difficult-to-treat patient population.

Immunogenicity results
Preliminary data show that HB-200 therapy is highly immunogenic, inducing unprecedented levels of activated, tumor antigen-specific CD8+ T cells. Immunogenicity data for eight patients with head and neck tumors were available at the time of data cut-off: six received HB-201 dose level 2 and two received alternating HB-201/HB-202 dose level 1. CD8+ T cell immunogenicity was assessed using direct Enzyme-Linked ImmunoSpot (ELISpot) T cell analysis and intracellular cytokine staining (ICS) followed by flow cytometry. ELISpot is used to quantify antigen-specific T cells in the blood whereas flow cytometry differentiates antigen-specific CD8+ T cells (killer T cells) from antigen-specific CD4+ T cells (helper cells). CD8+ T cells play a critical role in fighting cancer and infections.

At baseline, all patients had nearly undetectable levels of tumor-specific T cells. Within two weeks of a single dose of HB-200, all patients showed increased tumor-specific CD8+ T cell levels; all responses well exceeded the lower limit of quantification, and many approached the upper limit of quantification. Importantly, these results are based on direct ELISpot without ex vivo expansion of T cells, highlighting the magnitude of T cell response generated by HB-200 therapy. (Ex vivo expansion is often used to amplify responses otherwise not measurable).

Furthermore, flow cytometric analysis showed HB-200 therapy induced outstanding tumor-specific CD8+ T cell responses, including an average of 6 percent and up to 40 percent of the circulating T cell pool. (Of note, the latter was observed after alternating HB-201/HB-202 administration.) While there is no established threshold, a level of mid-single digit percentage, such as 5 percent, is a strong indicator of response. Both findings are consistent with pre-clinical observations, highlighting the potential of HOOKIPA’s proprietary arenaviral platform to deliver a new class of immunotherapeutics. The data are from the ongoing Phase 1 dose escalation; the recommended Phase 2 dose for HB-200 therapy has yet not been reached.

Translational results
Early translational data collected to-date suggest a relationship between T cells and clinical efficacy. Specifically, response rates and progression-free survival improve with higher dose levels and also with alternating, 2-vector therapy. In addition, paired biopsy data showed that HB-200 therapy induced similar increases in CD8+ T cells in both blood and tumor tissue. There is early evidence from tissue samples that HB-200 decreases immune suppression in the tumor microenvironment.

Preliminary efficacy results
As of the data cut-off, 15 patients with metastatic head and neck cancers were eligible for the efficacy analysis: 11 received HB-201 intravenously every three weeks and four received HB-201/HB-202 intravenously every three weeks. While treatment continues for these patients, the Phase 1 data show promising treatment duration with a median of 127 days for HB-201 recipients and 87 days for HB-201/HB-202 recipients at data cut-off. HB-201 dose level 2 may lead to prolonged treatment compared to dose level 1, whereas both dose levels of HB-201/HB-202 are ongoing.

Of the 15 patients, 93 percent (14/15 patients) had target lesion control, including 53 percent (8/15 patients) with target lesion reduction. Two of the 14 patients progressed at other sites, resulting in an overall disease control rate of 80 percent (12/15 patients). In particular, HB-201 monotherapy demonstrated an 18 percent overall response rate and an ongoing 3.45-month median progression-free survival (PFS). These results are particularly notable given the heavily pre-treated population (median of 3 prior treatments) and the historical lack of clinical response of active immunization therapies as monotherapies. In addition, HB-201 showed a 73 percent (8/11 patients) disease control rate, with two partial responses and six patients with stable disease, including four with stable disease for more than 16 weeks. Preliminary data on HB-201/HB-202 showed a disease control rate of 100 percent (4/4 patients).

Safety results
The Phase 1 data on 38 evaluable patients show that HB-200 therapy has a favorable safety profile in heavily pre-treated patients with HPV16+ cancers, underlining its potential as a monotherapy and in possible combination with checkpoint inhibitors. Treatment-related adverse events were reported in 53 percent of patients. There were no serious adverse events, no dose-limiting toxicities and no treatment-related adverse events rated grade 3 or higher. In addition, there were no discontinuations, dose changes or interruptions resulting from treatment-related adverse events. The most common side effects were fatigue (32 percent), fever (26 percent), nausea (18 percent) and hypertension (16 percent).

"Treatment options for patients with advanced HPV16+ cancers are limited, and there is no established standard of care following checkpoint inhibitor use," said Alan L. Ho, M.D., Ph.D., a medical oncologist at Memorial Sloan Kettering Cancer Center and a trial investigator. "Response rates are expected to decline with subsequent lines of therapy, so it’s encouraging to see an active immunization therapy, like HB-201 monotherapy, result in objective responses in heavily pre-treated patients. In addition, the unprecedented levels of antigen-specific CD8+ T cells induced by HB-201/HB-202 are promising and support the potential to convert immunogenicity into clinical efficacy."

Investor Event
HOOKIPA will host a live webcast event, "Advancing novel immunotherapies: HOOKIPA ASCO (Free ASCO Whitepaper) data review," today at 6:30 p.m. EDT. Joern Aldag, Chief Executive Officer, and Igor Matushansky, M.D., Ph.D., Chief Medical Officer, will provide an overview of the ASCO (Free ASCO Whitepaper) oral data and future plans for HOOKIPA’s oncology program. Dmitriy Zamarin, M.D., Ph.D., Translational Research Director in Gynecologic Medical Oncology at Memorial Sloan Kettering Cancer Center and a co-investigator in this study, will also offer commentary on the significance and implications of the translational findings. This event will be broadcast via Zoom Webinar and you may participate in the Q&A from Zoom.

To participate by phone, dial +1 (929) 205 6099 (US) or +44 330 088 5830 (International), webinar ID: 882 5139 3861# and press *9 when prompted to ask a question. The webcast and the presentation will be available within the Investors & Media section of HOOKIPA’s website at View Source A recording of the event will be available for 30 days.

About HB-201/HB-202
HB-201 and HB-202 are HOOKIPA’s lead oncology candidates engineered with the company’s proprietary replicating arenaviral vector platform. Each single-vector compound uses a different arenavirus backbone (Lymphocytic Choriomeningitis Virus for HB-201 and Pichinde Virus for HB-202), while expressing the same antigen, an E7E6 fusion protein derived from HPV16. In pre-clinical studies, alternating administration of HB-201 and HB-202 we observed in a ten-fold increase in immune response and better disease control than either compound alone.

About the trial (NCT04180215)
This Phase 1/2 clinical trial is an open-label trial exploring different dose levels and dosing schedules in individuals with treatment-refractory HPV16+ cancers who progressed on standard of care, including check point inhibitors. The primary endpoint of the Phase 1 is a recommended Phase 2 dose. Secondary endpoints include safety and tolerability, as well as preliminary efficacy defined by RECIST 1.1. The study also includes exploratory objectives on immunogenicity and pharmacodynamic biomarkers.

The trial is evaluating HB-201 as a monotherapy, as an alternating 2-vector therapy with HB-202, and in combination with a PD-1 inhibitor. Participants receive HB-201/HB-202 intravenously or, for patients with an accessible lesion, the first dose can be delivered via intratumoral injection followed by intravenous dosing. Dosing every three weeks and every two weeks is being explored, as well as different dose levels. Enrollment is ongoing and HOOKIPA expects to share additional clinical, translational and biomarker data at upcoming medical conferences.

About Human Papillomavirus
Human Papillomavirus, or HPV, is estimated to cause about 5 percent of the worldwide burden of cancers. This includes approximately 99 percent of cases in cervical, up to 60 percent of head and neck, 70 percent of vaginal and 88 percent of anal cancers.

The majority of these cancers are caused by the HPV serotype 16. Most infections with HPV are cleared from the body with no lasting consequences. However, in some cases, HPV DNA becomes integrated into chromosomal DNA. When host cells take up this DNA, they express the HPV E6 and E7 proteins. This uptake can potentially lead to cancer since expression of these proteins leads to alterations in cell cycle control, which in turn predisposes these cells to become cancerous.

Tollys presents scientific data supporting preclinical proof of concept for TL-532, its cancer immunotherapy drug candidate

On June 7, 2021 Tollys, a biopharmaceutical company developing TL-532, the first synthetic specific agonist of Toll-like Receptor 3 (TLR3) cancer immunotherapy, reported the presentation of a number of scientific results showing a preclinical proof of concept for TL-532 in the treatment of multiple cancers; at two online scientific conferences (Press release, Tollys, JUN 7, 2021, View Source [SID1234583651]).

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Doctors Marc Bonnin and Sylvain Thierry will present Tollys’ results at the European Association of Cancer Research’s EACR 2021 Congress, which will take place from June 9 -12:

Dr Marc Bonnin, head of the discovery unit at Tollys, will present ‘Discovery process and in vitro biological characterization of rationally designed TL-532 Toll-like Receptor 3 (TLR3) agonist as anti-cancer molecule’ (EACR21v-0484)
Dr Sylvain Thierry, head of translational research at Tollys, will present ‘First rationally designed Toll-like Receptor 3 (TLR3) agonist TL-532, induces apoptosis specific of tumor cells and long-lasting anti-tumor specific immunity’ (EACR21v-0469)
These presentations will cover the main preclinical results obtained with TL-532, in particular:

How it differs from all TLR ligand receptors studied to date
Direct and selective apoptosis induction of tumor cells in vitro and ex vivo on tumor samples from patients
Prevention of recurrence through immunological memory; triggered and maintained in the long term by TL-532, as demonstrated in a rodent model
Immunological switch in the tumor microenvironment in patients undergoing tumor resection
"We’re proud to be able to share this data, which proves the potential of this specific TLR3 agonist in immuno-oncology, in particular by releasing tumor-specific antigens. We believe these results are highly promising and we are looking forward to sharing them with the scientific community," said Dr Bettina Werle, chief scientific officer at Tollys.

Dr Werle was also invited to present some initial results at the Sting & TLR Targeted Therapies summit. Her presentation took place on May 27, 2021: ‘TL-532, the First Rationally Designed TLR3 Agonist Creates Long-Lasting Tumor Specific Immunity In Vivo’.

About TL-532

TL-532 is a specific TLR3 agonist with a triple mechanism of action: it induces 1) the death by apoptosis of cancer cells, leading to the release of tumor specific antigens, 2) activation of the immune system to mount a specific T-cell response against the tumor antigens and 3) a tumor microenvironment switch by producing cytokines and chemokines which are unfavorable to tumor development. The result is the immunogenic death of cancer cells and an auto-vaccination preventing the recurrence of cancer. This TLR3 receptor is very different from other TLRs tested to date (TLR 2, 4, 7, 8, 9) due to this unique mechanism of action which simultaneously combines immune stimulation with its specific apoptotic effect on cancer cells.

While the TLR3 receptor is a validated cancer target, TLR3 agonists have yet to reach the market. TL-532 is the first synthetic specific TLR3 agonist with a defined – and patented – double-stranded RNA sequence. As such, TL-532 has the potential to be best-in-class and first-to-market.

bluebird bio to Present at Goldman Sachs Global Healthcare Conference

On June 7, 2021 bluebird bio, Inc. (NASDAQ: BLUE) reported that members of the management team will participate in the Goldman Sachs 42nd Annual Global Healthcare Conference, Tuesday, June 8, at 8:50 a.m. ET (Press release, bluebird bio, JUN 7, 2021, View Source [SID1234583650]).

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To access the live webcast of bluebird bio’s presentation, please visit the "Events & Presentations" page within the Investors & Media section of the bluebird bio website at View Source A replay of the webcast will be available on the bluebird bio website for 90 days following the event.

Janssen Affiliate Cilag GmbH International Discontinues Collaboration and License Agreement with argenx for Cusatuzumab

On June 7, 2021 Cilag GmbH International, one of the Janssen Pharmaceutical Companies of Johnson & Johnson, reported its decision not to continue the collaboration and license agreement with argenx for cusatuzumab, an investigational therapeutic antibody that targets CD70 (Press release, Johnson & Johnson, JUN 7, 2021, View Source [SID1234583649]).

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The decision is based upon Janssen’s review of all available cusatuzumab data and in consideration of the evolving standard of care for the treatment of acute myeloid leukemia (AML). Final results from Janssen’s clinical studies of cusatuzumab will be presented in the future.

Janssen will work with argenx to transition the cusatuzumab program back to argenx. Patients currently enrolled in ongoing cusatuzumab clinical trials will continue to be supported through treatment and follow-up.

Janssen entered into the worldwide collaboration and license agreement with argenx in December 2018 to develop and commercialize cusatuzumab in AML and potential additional indications.

Seven and Eight Biopharma’s BDB001 in Combination with Pembrolizumab Shows Favorable Safety and Clinical Responses in Interim Phase 1 Data Presented at the 2021 ASCO Annual Meeting

On June 7, 2021 Seven and Eight Biopharmaceuticals Inc., a clinical stage biotechnology company developing proprietary novel immuno-oncology therapies to activate the immune system against cancer, reported the presentation of Phase 1 data for BDB001 in combination with pembrolizumab in advanced solid tumors at the 2021 American Society of Clinical Oncology (ASCO) (Free ASCO Whitepaper) Annual Meeting (Press release, Seven and Eight Biopharmaceuticals, JUN 7, 2021, View Source [SID1234583648]).

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BDB001 is an immune modulator capable of activating dendritic cells to initiate both innate and adaptive immunity against cancer. BDB001 is a first-in-class TLR7/8 agonist delivered intravenously, allowing for broader treatment of solid tumors. Previously, Seven and Eight Biopharma reported that intravenous administration of BDB001 as monotherapy showed favorable tolerability and robust systemic immune activation leading to durable clinical responses.

The poster discussion session at ASCO (Free ASCO Whitepaper) for Abstract #2512 revealed new interim safety and efficacy results for a Phase 1 dose escalation / expansion trial of BDB001 in combination with pembrolizumab in advanced solid tumors (NCT03486301). The results show that BDB001 in combination with pembrolizumab was well tolerated, and induced robust immune activation leading to clinical responses. Based on these results, the recommended Phase 2 dose (RP2D) of BDB001 was determined and is currently being further evaluated in an ongoing dose expansion phase.

"It is encouraging to see that BDB001 in combination with pembrolizumab can be safely delivered intravenously and produces clinical responses in heavily pre-treated tumors" said lead author and study investigator Dr. Manish R. Patel, of Florida Cancer Specialists/Sarah Cannon Research Institute.

"These promising interim results show that BDB001 in combination represents a novel and viable treatment for advanced solid tumors. It is especially encouraging to see responses in PD-L1 negative and refractory tumors" said Dr. Robert H.I. Andtbacka, Chief Medical Officer, Seven and Eight Biopharma. "We continue to enroll subjects in the dose expansion part of this trial, to further evaluate safety, efficacy, and immune modulatory effects in the tumor microenvironment."

"We are very excited about the clinical data for BDB001 in combination with pembrolizumab, as we continue to advance our robust immuno-oncology pipeline in treatments beyond anti-PD-(L)1, including preclinical platform programs in TLR Ligand Antibody Conjugation" said Dr. Walter Lau, Chief Executive Officer, Seven and Eight Biopharma.

Presentation Details:

Abstract Title: BDB001, an intravenously administered toll-like receptor 7 and 8 (TLR7/8) agonist, in combination with pembrolizumab in advanced solid tumors: Phase 1 safety and efficacy results.

Abstract Authors: Manish R. Patel, Anthony W. Tolcher, Drew W. Rasco, Melissa Lynne Johnson, Angela Tatiana Alistar, Lixin Li, Alexander H. Chung, Robert H.I. Andtbacka

Session Title: Poster Discussion Session, Developmental Therapeutics—Immunotherapy

On-Demand Session Release Date and Time: 6/4/2021, 9:00 AM-10:00 AM

Abstract Number: 2512

The poster presentation will be available on the ASCO (Free ASCO Whitepaper) Meeting Library and on the Company’s website at www.7and8biopharma.com.

Abstract Summary:

– Seven and Eight Biopharma’s systemic delivery of the TLR 7 and 8 dual agonist BDB001 is first in class.

– BDB001 was delivered safely intravenously in combination with pembrolizumab.

– BDB001 in combination with pembrolizumab showed robust dose dependent immune activation without increased risk of CRS, as evidenced by minimal increase in pro-inflammatory/CRS cytokines, IL-6, IL-10, and TNF-α.

– Overall, BDB001 was well tolerated and over 21% of subjects did not have any treatment related adverse events. There were few Grade 3 and no grade 4 or 5 adverse events.

– At BDB001 Levels 3 and 4, 19 subjects were evaluable for efficacy. There was evidence of:

Rapid and deep clinical responses were observed in tumors with low response rate to anti-PD-1 therapy based on their PD-L1 negative, MSI-stable, and TMB-low status.

5 clinical responses including 1 Complete Response (CR)

Overall Response Rate (ORR) was 26%; Disease Control Rate (DCR) of 58%

Clinical responses were seen in subjects with cholangiocarcinoma, hepatocellular carcinoma, melanoma, ovarian carcinoma, and triple negative breast cancer.

Robust anti-tumor immune activation via IP-10 (CXCL10) upregulation, which correlated with clinical responses.

– BDB001 in combination with pembrolizumab is a promising novel therapeutic option for patients with advanced solid tumors and is being evaluated in an ongoing dose expansion trial