Oncologie Announces New Data and Analyses from Clinical Programs and Name Change to OncXerna Therapeutics

On September 18, 2020 Oncologie, Inc., a precision medicine company using an innovative RNA-based biomarker platform to predict patient responses for potentially first-in-class targeted oncology therapies, announced new data and analyses from its lead clinical programs, bavituximab and navicixizumab (Press release, OncXerna Therapeutics, SEP 18, 2020, View Source [SID1234572120]). On the basis of these positive data, the company also announced its rebranding to OncXerna Therapeutics, Inc., a change that reinforces the company’s focus on using its RNA-based approach to guide novel, targeted treatments to specific people with cancer.

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"With a deep understanding of the tumor microenvironment biology at the RNA-level through our novel biomarker panel, we aim to dramatically improve clinical outcomes by matching patients to therapies with a mechanism of action that targets that specific biology," said Laura Benjamin, Ph.D., President and Chief Executive Officer at OncXerna Therapeutics. "Today’s results demonstrate a clear ability of our first panel to distinguish responders versus non-responders in our bavituximab and navicixizumab programs, and we are excited to deploy this approach in the next prospectively-defined trials that could support registration."

Interim results from Phase 2 (ONCG100) trial of bavituximab and KEYTRUDA

Trial design and background:

The Phase 2 (ONCG100) trial is a multicenter, open-label, single-arm global trial designed to assess the safety, tolerability, and antitumor activity of the investigational agent bavituximab, a chimeric monoclonal antibody that targets phosphatidylserine, in combination with KEYTRUDA, Merck’s anti-PD-1 therapy, in patients with advanced gastric and gastroesophageal cancer who have progressed on or after at least one prior standard therapy. Bavituximab previously demonstrated clinical activity in a post-hoc subset analysis in patients with non-small cell lung cancer (NSCLC) who were given a PD-1 inhibitor following bavituximab treatment, suggesting that a treatment combination of bavituximab and a PD-1 inhibitor could generate similar activity in a prospective clinical trial. In addition to measuring safety and antitumor activity in this trial, OncXerna is deploying its proprietary RNA biomarker platform (TME Panel-1) to identify patients based on their response to treatment and the dominant biology of their tumor microenvironment with the potential to dramatically improve outcomes in the next, prospectively designed trial.

Approximately 80 patients in the U.S., United Kingdom, South Korea and Taiwan are planned for enrollment in two separate groups of patients: Checkpoint inhibitor-naïve and checkpoint inhibitor-relapsed. The trial is continuing to enroll both groups with planned updates from all patients during the first half of 2021.

Interim results:

Interim results provided today, from the first 36 patients enrolled and with a post-baseline scan in the checkpoint inhibitor-naïve group, include the following:

Patient demographics: Mean age of 61 years (55% non-Asian/45% Asian) with approximately 70% and 30% of patients receiving their second-line and third-line of treatment, respectively. In terms of mutation status, known MSI-H patients were excluded (MSS included) and enrollment was PD-L1 agnostic, with 25% of patients PD-L1 negative.

Safety and tolerability: Bavituximab and KEYTRUDA treatments were well tolerated with 90% of treatment emergent adverse events considered Grade 1-3. Fourteen patients had at least one serious adverse event (SAE). All SAEs were reported as not related to bavituximab and KEYTRUDA except for pneumonitis in one patient that resolved and was considered related to the combination of bavituximab and KEYTRUDA.

Efficacy measures: Bavituximab and KEYTRUDA achieved an overall response rate (ORR) of 19% (7/36) in the evaluable population and 43% (3/7) in exploratory analyses of patients with a low neutrophil-to-lymphocyte (NLR) ratio (<4) and identified as biomarker positive using OncXerna’s TME Panel-1. In a clinical trial of KEYTRUDA that led to an accelerated approval in the third-line setting, the ORR was 13% with a 16% ORR in PD-L1 positive patients and a 9% ORR in MSS patients. Treatment with bavituximab and KEYTRUDA also generated a complete response in 20% (2/10) of patients who were PD-L1, CPS<1; a patient population where KEYTRUDA historically generates very low complete responses. In terms of response duration, all confirmed responders remain in the trial, with the longest responder approaching one-year of duration of response.

Next steps:

These data are being presented at the European Society for Molecular Oncology (ESMO) (Free ESMO Whitepaper) Virtual Congress 2020 taking place September 19-21, 2020.

OncXerna plans to conduct additional clinical trials designed to prospectively enrich for TME Panel-1 biomarker positive patients, as well as to explore additional solid tumor types.

OncXerna biomarker analysis from Phase 1b trial evaluating navicixizumab in ovarian cancer

Previously announced data and background:

OncXerna’s navicixizumab is a bispecific antibody designed to inhibit both Delta-like ligand 4 (DLL4) in the Notch cancer stem cell pathway as well as vascular endothelial growth factor (VEGF). Interim data from a Phase 1b dose escalation and expansion trial of navicixizumab plus paclitaxel in 44 platinum-resistant ovarian cancer patients who had failed more than two prior therapies and/or received prior Avastin (bevacizumab) therapy were presented virtually at the 2020 Society of Gynecologic Oncology (SGO) Annual Meeting in May 2020. Treatment with navicixizumab and paclitaxel demonstrated an ORR of 43% in all patients, and 64% and 33% in bevacizumab-naïve, and bevacizumab pre-treated patients, respectively. Treatment-related adverse events were manageable and included hypertension (58%), headache (29%), fatigue (26%) and pulmonary hypertension (18%).

Updated biomarker analyses and results:

Using its RNA-based biomarker TME Panel-1, OncXerna recently analyzed patient tissue samples obtained from 28 of the 44 patients from the Phase 1b trial. Results from this analysis revealed the following:

Clinically meaningful improvement in median progression-free survival (PFS) of 9.2 months for TME Panel-1 biomarker positive patients (n=10) compared with a median PFS of 3.5 months for biomarker negative patients (n=13), hazard ratio (0.276). The confirmed ORR for TME Panel-1 biomarker positive patients (n=10) was 70% compared to 31% ORR for TME Panel-1 biomarker negative patients (n=13).

Patients in the TME Panel-1 biomarker positive panel achieved a 70% ORR, and excluded all who had progressive disease, compared with a 31% ORR for patients in the TME Panel-1 biomarker negative panel. In Avastin-experienced patients, achievement of a 71% ORR and 100% disease control rate (DCR) in TME Panel-1 biomarker positive patients (n=7) compared with 25% ORR and 50% DCR achieved in biomarker negative patients (n=8) (Table 1).


Table 1: TME Panel-1 Results from Phase 1b trial of Navicixizumab plus placlitaxel in patients with late-stage ovarian cancer

Avastin Naïve and Experienced
Confirmed Clinical Response (%) Biomarker positive (n=10) Biomarker negative (n=13)
ORR 70% 31%
DCR 100% 69%
CR 0% 8%
PR 70% 23%
SD 30% 39%
PD 0% 31%

Avastin Experienced
Confirmed Clinical Response (%) Biomarker positive (n=7) Biomarker negative (n=8)
ORR 71% 25%
DCR 100% 50%
PR 71% 25%
SD 29% 25%
PD 0% 50%
"Biomarker" refers to TME Panel-1

Next steps:

As a result of these analyses, OncXerna plans to conduct additional clinical trials designed to prospectively enrich for TME Panel-1 biomarker positive patients with ovarian cancer who are platinum-resistant and Avastin-experienced to support registration, as well as to explore additional solid tumor types.

About Bavituximab

Bavituximab is an investigational antibody that reverses immune suppression by inhibiting phosphatidylserine (PS) signaling and is currently in Phase 2 clinical trials to treat a specific subset of patients with advanced gastric cancer to improve their response to anti-PD-1 treatment. The mechanism of action of bavituximab is to block tumor immune suppression signaling from PS to multiple immune cell receptor families (e.g., TIMs and TAMs). The dominant biology targeted by bavituximab may be relevant for patients with many types of solid tumors whose immune systems are too suppressed to benefit from currently available immune oncology therapies. Our clinical trials currently combine bavituximab with KEYTRUDA to test the hypothesis that relieving immunosuppression can enhance responses to checkpoint inhibitors. Bavituximab is an investigational agent that has not been licensed or approved anywhere globally, and it has not been demonstrated to be safe or effective for any use, including for the treatment of advanced gastric cancer.

About Navicixizumab

Navicixizumab is an investigational anti-DLL4/VEGF bispecific antibody that has demonstrated antitumor activity in patients who have progressed on Avastin (bevacizumab) in a Phase 1a/b clinical trial. The U.S. Food and Drug Administration granted Fast Track designation to navicixizumab for the treatment of high-grade ovarian, primary peritoneal or fallopian tube cancer in patients who have received at least three prior therapies and/or prior treatment with Avastin. OncXerna is targeting patients whose dominant tumor biology is driven by angiogenesis with a focus beyond VEGF to include broader anti-angiogenic pathways. Navicixizumab is an investigational agent that has not been licensed or approved anywhere globally, and it has not been demonstrated to be safe or effective for any use, including for the treatment of advanced ovarian cancer.

LamKap Bio Group and Lonza Collaborate

On September 18, 2020 LamKap Bio Group and Lonza reported that it Collaborate to Manufacture Bispecific Antibodies for Cancer Treatment (Press release, LamKap Bio Group, SEP 18, 2020, View Source [SID1234565465]).

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LamKap Bio Group develops fully human bispecific κλ antibodies targeting malignant cells in solid cancers
Lonza to provide cell line development, drug substance and drug product services and cGMP manufacturing for two programs
Lonza’s LightPath cell line development program was optimized to ensure improved process yield and throughput
Quote from Shiva Khalafpour, VP, Head of Commercial Mammalian and Microbial Development and Manufacturing, Lonza:
"Lonza’s subject matter experts enjoyed working with LamKap’s technical team to identify specific molecule needs and design a tailored work package suitable to achieve their goals. This included a customized cell line development program based on Lonza’s GS Gene Expression System and LightPath CLC methodology and optimization of the customer downstream purification approach in order to facilitate manufacturing. "

Quote from Klaus Strein, Chairman of the LamKap Bio Group:
The LamKap Bio Group together with its strategic partner Light Chain Biosciences/NovImmune have considerable experience in the R&D of T-cell bispecific antibodies and tumor targeted anti-CD47 bispecific antibodies. Technical development and GMP manufacturing of both types of bispecific antibodies were already successfully performed by Lonza in the recent years. The new collaboration with Lonza is an important pillar in the development of two Clinical Leads.

Basel and Pfäffikon, Switzerland, 17 September 2020 – LamKap Bio Group, a biotechnology group focused on the research, development and manufacturing of tumor-targeted antibody-based therapies, and Lonza announced today that the companies have a development and manufacturing collaboration in place to support their current and future product pipeline. Lonza will provide cell line and process development, drug substance manufacturing and drug product services of LamKap’s two fully human bispecific antibody products, NILK-2301 and NILK-2401.

LamKap’s therapeutic bispecific antibodies are engineered to bind to two different antigens simultaneously. The two antigens can be either located on one cell type, e.g., a tumor cell, or two different cell types, e.g., on a tumor cell and an immune effector cell. Both NILK-2301 and NILK-2401 can be used as monotherapy and/or in combination. NILK-2301 binds to a tumor-associated antigen (TAA) and CD3 on T-cells, re-targeting T cells to kill tumor cells. NILK-2401 is also targeted to a TAA and in addition to CD47 on tumor cells, thus causing increased antibody-dependent cellular phagocytosis (ADCP) and antibody-dependent cell-mediated cytotoxicity (ADCC).

Using LamKap’s fully human bispecific Kappa Lambda antibodies (κλ), consisting of two identical heavy chains, a kappa (κ) and a lambda (λ) light chain and an IgG1 Fc, helps the human body to fight cancer. This structure is nearly identical to the structure of a standard IgG antibody and lowers the risk of inducing immunogenicity while minimizing the loss of exposure. Antibodies in this format are ideally suited for therapeutic application in both benign and malignant diseases. The κλ format facilitates production/purification.

Building upon Lonza’s previous experience with the κλ body program, as well as several other bispecific antibody platforms and the extensive upstream and downstream processing know-how, Lonza will carry out cell line construction and cGMP drug substance manufacturing at its Slough, UK and Hayward, US sites. The LightPath cell line development program will start in Q3 2020, providing LamKap with material to enter phase I clinical studies. The early-stage drug product formulation and stability studies will be performed at Lonza’s Drug Product Services facility in Basel, Switzerland.

The scope of the package was tailored to ensure the program could meet the requirements of large-scale manufacturing of unique κλ body products.

Immutep Reports Improving Results from INSIGHT-004 Trial

On September 18, 2020 Immutep Limited (ASX: IMM; NASDAQ: IMMP) reported further interim data from its ongoing INSIGHT-004 Phase I clinical trial (Press release, Immutep, SEP 18, 2020, View Source [SID1234565422]). The data were presented at the ESMO (Free ESMO Whitepaper) Virtual Congress 2020 on 17 September 2020, CEST (poster ID number 1032P) by trial investigator at Institute of Clinical Cancer Research, Krankenhaus Nordwest (IKF), PD Dr. Thorsten Götze.

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INSIGHT-004 is evaluating the combination of Immutep’s lead product candidate, eftilagimod alpha ("IMP321" or "efti") with avelumab (Bavenico), a human anti-PD-L1 antibody, in 12 patients with different solid tumours, primarily gastrointestinal. It is being conducted under Immutep’s collaboration with Merck KGaA, Darmstadt, Germany, and Pfizer Inc., which are co-developing and co-commercialising avelumab. INSIGHT-004 is the fourth arm (Stratum D) of the investigator-initiated INSIGHT trial which is conducted by IKF in Frankfurt, Germany.

Prof Salah-Eddin Al-Batran, INSIGHT-004 trial investigator and Director of IKF said: "It is encouraging to see the range of patients with different solid cancers that are responding to the combination of efti and avelumab, including PD-L1-negative cervical cancer, squamous anal cell carcinoma and mesothelioma. These tumours are not typically responsive to immune checkpoint therapy and warrant further investigation."

Results Summary (data cut off 12 June 2020)

41.7% of patients (5 / 12) showed a partial response (PR) to the combination therapy according to RECIST 1.1. Previously 33% showed a PR (June 2020).

Encouraging durable deep responses in PD-L1 negative cancer.

Includes 2 patients with clinical progression

**
Response assessment not yet performed

Immutep Limited, Level 12, 95 Pitt Street, Sydney NSW 2000

ABN: 90 009 237 889

Safety

Interim results from INSIGHT-004 show that the combination of efti and avelumab is well tolerated with no dose limiting toxicities, building on efti’s strong safety profile to date.

IKF INSIGHT Trial Poster

IKF also presented data from the broader INSIGHT trial at ESMO (Free ESMO Whitepaper) showing that intratumoral and intraperitoneal administration of efti up to 30 mg displayed signals of clinical and cytokine responses. Both IKF posters are appended below and are available on the Company’s website at View Source

About INSIGHT-004

INSIGHT-004 is the fourth arm of the investigator-initiated INSIGHT trial which is being conducted by the Institute of Clinical Cancer Research IKF at Krankenhaus Nordwest in Frankfurt. It is being conducted under Immutep’s collaboration with Merck KGaA, Darmstadt, Germany, and Pfizer Inc., and is evaluating the safety, tolerability and recommended Phase II dose of efti when given in combination with avelumab. It is the first combination trial of an approved and marketed anti-PD-L1 drug and efti.

Patients in cohort 1 receive 6mg doses of efti every two weeks with the standard dose of avelumab (800mg every two weeks), while patients in cohort 2 receive a higher dose of efti, 30mg, with avelumab.

LinkDoc Raises $103 Million for Oncology AI/Big Data Services

On September 18, 2020 LinkDoc Technology, a Beijing oncology big data company, reported that it raised $103 million in a Series D+ funding round, primarily from new investors, CICC Capital, Youshan Capital and iFOF (Press release, LinkDoc, SEP 18, 2020, View Source [SID1234565413]). Founded in 2014, LinkDoc offers electronic medical records to hospitals, and it gathers medical data, using AI to develop clinical best-practice guidelines for cancer. Two years ago, LinkDoc completed a $143 million Series D round exclusively from state-owned China Investment Corporation.

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New Data Gives Hope to Small Cell Lung Cancer Patients

On September 18, 2020 EORTC reported that About 13% of lung cancer patients have Small Cell Lung Cancer (SCLC) (Press release, EORTC, SEP 18, 2020, View Source [SID1234565398]). The prognosis of this disease is very poor with 5-year survival rates of 31% for limited-stage SCLC (LS-SCLC) and 2% for extensive-stage SCLC (ES-SCLC). However, recent studies have shown that anti PD-L1 antibodies can extend overall survival of ES-SCLC patients when combined with platinum-etoposide treatment.

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Professor Benjamin Besse, Head of the Cancer Medicine Department at Gustave Roussy Cancer Campus and Professor of Medical Oncology at Paris-Saclay University, Orsay, presented the late breaking data from EORTC-1417-LCG REACTION study: a phase II study of etoposide and cis/carboplatin with or without pembrolizumab in untreated extensive small cell lung cancer at the ESMO (Free ESMO Whitepaper) Virtual congress today.

All 125 patients (61 in experimental vs 64 in control arm) recruited previously responded to 2 cycles of platinum-etoposide. They were randomized into the control arm of 4 additional cycles of platinum-etoposide treatment or the experimental arm with 4 additional cycles of platinum-etoposide treatment combined with pembrolizumab and then up to 35 cycles of pembrolizumab. 119 (58 vs 61) patients were eligible and started at least one dose of the treatment. 19 patients had crossed over to the experimental arm at the time of progression. In the experimental arm, 43 % exhibited grade 3 to 5 adverse events vs 36% in the standard arm, median progression free survival was 4.7 vs. 5.4 months and overall survival was 12.3 vs 10.4 months respectively. Besse concluded that even though the combination of etoposide and platinum with pembrolizumab was well tolerated, it did not improve progression free survival compared to standard treatment. However, the data did elude to the potential increase in overall survival, it should be noted that pembrolizumab needs to be introduced as first line treatment in order to benefit from this improvement.

"In REACTION, immunotherapy was added from the third cycle of chemotherapy," said Besse. "Our results confirm the benefit of adding immunotherapy to first line chemotherapy in patients with extended SCLC. Our strategy is interesting for patient with PS2 at cycle 1 (thus unfit for immunotherapy) that will improve to PS 1 or 0 at cycle 3".

Mini Oral Session – Non-metastatic NSCLC and other thoracic malignancies

LATE BREAKING ABSTRACT: REACTION: A phase II study of etoposide and cis/carboplatin with or without pembrolizumab in untreated extensive small cell lung cancer