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Monday, November 4, 2019

SITC 2019 preview – Pieris joins the quest for a better Herceptin

Any signs of efficacy with PRS-343 could help Pieris claw back some of its recent losses, but Her2 targeting is increasingly competitive.
Pieris Pharmaceuticals’ lead immuno-oncology asset, PRS-343, has so far flown under the radar. This might be about to change, with the 4-1BB and Her2-targeting bispecific set to feature in a late-breaking presentation at the Society of the Immunotherapy of Cancer conference on Friday.
The findings will be early but analysts hope to see some evidence of activity in the form of response rates. With many other companies vying to develop next-generation Her2-targeting agents, Pieris will have to hope that its different approach will sets PRS-343 apart.
Reducing toxicity?
Activating 4-1BB stimulates a T-cell response, but previous efforts to harness this mechanism have led to liver toxicity. By homing in on Her2-positive cancer cells, PRS-343 is designed to limit the immune response to the tumour microenvironment; the hope is that this will help the project avoid these side effects.
The subject of the SITC presentation is a phase I dose-escalation trial in patients with various advanced Her2-positive solid tumours including breast, gastric and bladder cancers. So far only the title has been disclosed; Pieris has said that it plans to present comprehensive pharmacokinetic, safety, tolerability and biomarker data at the meeting.
Evercore ISI analysts are also hoping to see some data on response rates, noting that Pieris has implied that “at least some” patients responded to PRS-343.
In a bigger trial, a meaningful bar to hit would be around 15% in metastatic breast cancer, in line with what Herceptin monotherapy can achieve in heavily pre-treated patients, and 20% in gastric cancer, similar to that seen with immunotherapy.
However, the upcoming data will be tricky to interpret given the small number of patients in each PRS-343 dosing group. A more realistic expectation, according to Evercore, would be to see “at least a few responses” in breast and bladder cancer patients at the high doses being tested.
Another thing to watch out for will be any signs that PRS-343 could be turning “cold” tumours “hot”, indicated by increased infiltration of cytotoxic T cells into the tumour. This could be particularly important for PRS-343’s chances as a combination therapy – a phase I trial testing the project in combination with Roche’s Tecentriq is also ongoing.
Her2 rush
Still, Pieris is far from the only company looking at Her2. The most advanced of the industry’s efforts to produce a better Herceptin is Astrazeneca and Daiichi’s antibody-drug conjugate trastuzumab deruxtecan, which is expecting a US approval decision in the second quarter.
This project is forecast to be the most valuable next-gen Her2 project, according to EvaluatePharma sellside consensus; indeed, it is currently considered the sector’s most valuable oncology R&D project by some way.
SELECTED MID-TO-LATE-STAGE NEXT-GEN HER2-TARGETING PROJECTS
ProjectCompanyDescriptionSetting & trial details2024e sales ($m)
Filed
Trastuzumab deruxtecan/DS-8201Astrazeneca/
Daiichi Sankyo
Anti-Her2 antibody drug conjugateMetastatic breast cancer, approval decision due in Q2 20202,719
Phase III
TucatinibSeattle GeneticsHer2-selective TKIMetastatic breast cancer, Her2Climb trial reported320
PyrotinibJiangsu Hengrui MedicineEGFR & Her2 dual kinase inhibitorMetastatic breast cancer, China trials ongoing inc Herceptin combo381
MargetuximabMacrogenicsAnti-Her2 Fc-optimised MAbMetastatic breast cancer, Sophia trial reported319
TAK-788TakedaEGFR & Her2 dual kinase inhibitor1L NSCLC with EGFR exon 20 insertions, phase III not yet recruiting134
VarlitinibAslan PharmaceuticalsPan-Her inhibitorMetastatic biliary tract cancer, data from Treetopp trial imminent4
SYD985/trastuzumab duocarmazineSynthonAnti-Her2 MAb-duocarmycin conjugateBreast cancer, Tulip trial ongoing
BAT8001Bio-Thera SolutionsAnti-Her2 MAb-maytansinoid conjugateMetastatic breast cancer, China trial ongoing
Phase II
MCLA-128/zenocutuzumabMerusAnti-Her2 & Her3 bispecific antibodyNRG1 fusion cancers; focus now on pancreatic & NSCLC320
TesevatinibKadmonEGFR, Her2 & VEGFR kinase inhibitorGlioblastoma247
ZW25ZymeworksHer2 x Her2 bispecificGastroesophageal adenocarcinoma89
AE37 VaccineGenerex BiotechnologyAnti-Her2 vaccineTNBC in combo with Keytruda
Neuvax/nelipepimut-sSellas Life ScienceAnti-Her2 vaccineBreast cancer in combo with Herceptin
Source: EvaluatePharma, clinicaltrials.gov.
As for the chasing pack, hopes are rising for Seattle Genetics’ tucatinib after the company recently reported a win in the Her2Climb trial; a filing in third-line Her2-positive metastatic breast cancer is slated for the first quarter of 2020.
But another Her2 hopeful, Macrogenics, might struggle to find a niche for its candidate margetuximab. The latest overall survival data from the Sophia trial failed to impress, and the project could end up being reserved for patients already treated with trastuzumab deruxtecan and tucatinib, Leerink analysts reckon.
Meanwhile, Merus has switched focus with its Her2 and Her3-targeting bispecific – it had been testing the compound in breast and colorectal cancer, but has now homed in on pancreatic and non-small cell lung cancer patients with NRG1 fusions following positive early findings in this group, which were presented at the Triple Meeting.
Zymeworks also had data at that conference, from a phase I study of its bispecific ZW25. The project is designed to bind to two different locations on Her2 with the aim of increasing potency – Zymeworks makes the bold claim that the asset could be the best-in-class Her2-targeting antibody. The group plans to put this to the test with a phase III trial slated for next year pitting ZW25 against Herceptin in first-line gastro-oesophageal adenocarcinoma.
Against this backdrop, Pieris might have its work cut out to find a niche, and the stakes are particularly high for the company after phase I data with the inhaled IL-4 antagonist PRS-060 sent its share price tumbling in September. Still, any positive signs with PRS-343 could give the beleaguered group a boost.

Daiichi Sankyo leaves US pain market amid oncology pivot, opioid scrutiny

Daiichi Sankyo’s short-lived interest in the U.S. pain management market has officially come to an end, as the company’s new CEO continues shifting its focus to oncology and the industry reels from the nation’s opioid crisis.
The Japanese pharma handed the opioid-induced constipation treatment Movantik back to AstraZeneca as of October, and it told Inspirion Delivery Sciences to cancel their licensing agreement covering opioid drugs MorphaBond and RoxyBond, Daiichi Sankyo’s newly minted CEO Sunao Manabe told investors during a call Thursday.
“With these actions, [Daiichi Sankyo’s U.S. operation] exited the pain treatment business and focused on oncology and [the] injectable iron business,” he said.
It’s not immediately clear how the exit affects Daiichi’s U.S. sales force, but, according to a WARN notice posted in August, Daiichi’s U.S. outfit had planned to cut 68 employees in New Jersey effective Oct. 7. The company didn’t respond to a FiercePharma request for confirmation by publication time.
The moves mark a change of course at Daiichi. In its annual report for the fiscal year ended in March, the company had said it would “seek growth” of both Movantik and MorphaBond and planned to work out a delayed launch of RoxyBond after a rival company challenged the FDA’s approval of the drug in a lawsuit.
As it slims down in the messy pain management market, Daiichi is doubling down on oncology. While Daiichi and AZ have cut ties on Movantik, they recently inked an oncology pact, with AZ betting $6.9 billion on Daiichi’s lead antibody drug conjugate (ADC), [fam-] trastuzumab deruxtecan (DS-8201), in HER2-expressing cancers. An application for the drug in metastatic breast cancer has just been put under FDA priority review, with a decision expected in the second quarter of 2020.

The deal is a huge endorsement for Daiichi’s ambition of becoming a “global pharma innovator with competitive advantage in oncology” by 2025. Under that project, Daiichi in February 2018 said it would reorganize its U.S. commercial organization in preparation for upcoming oncology launches. At that time, the company planned to reduce headcount by about 280 employees.
As the first project, Daiichi in August nabbed an FDA green light—its first U.S. cancer nod since 2011—for Turalio for adults with a rare joint cancer known as tenosynovial giant cell tumor.
On the manufacturing side, Manabe said the company plans to invest JPY 100 billion ($920 million) or more “to be prepared for the increase in demand of ADC franchise’s investigational drugs and products.”

Daiichi’s dabbling in the U.S. painkiller market can be traced back to 2014, when it agreed to pay up to $650 million for some hydrocodone combo medications from Charleston Laboratories. However, the alliance was cut short in 2017 after the FDA shot down the pair’s lead project, CL-108. Daiichi took a $250 million impairment charge for abandoning the deal.
Hoping to build its U.S. pain portfolio into a blockbuster franchise, the Japanese company had by that time licensed U.S. rights to Inspirion’s FDA-approved extended-release morphine formulation MorphaBond and what would later be branded as Roxybond, an immediate-release form of oxycodone hydrochloride. Both drugs feature a unique abuse-deterrent technology that resists passage through a syringe needle.
The Movantik pact with AZ was formed in 2015, with Daiichi paying $200 million upfront for co-marketing rights. But the drug hasn’t exactly been a gold mine. In the first three quarters, its sales only reached $70 million in the U.S., down 14% over the prior year, according to AstraZeneca.

The news came as U.S. opioid players Johnson & Johnson, Teva and Purdue Pharma offered up multibillion-dollar settlements for their roles in the U.S. opioid epidemic.
Meanwhile, Daiichi is holding onto the pain business in its home country. In April, it launched Tarlige (mirogabalin) in Japan for peripheral neuropathic pain to challenge Pfizer’s blockbuster Lyrica. And in September, it rolled out in the country a new generic formulation of oxycodone hydrochloride for sustained cancer pain treatment.

FibroGen down 6% on bearish Plainview report

FibroGen (FGEN -5.5%) slips on below-average volume in early trade in apparent response to a bearish report from Plainview LLC who questions the safety profile of lead drug roxadustat and efficacy of candidate #2 pamrevlumab.
Plainview says the rate of major adverse cardiovascular events (MACE), a composite measure of all-cause mortality, heart attacks and strokes, associated with roxadustat may not be as good as erythropoietin (EPO) analogs (e.g., Amgen’s Epogen) in dialysis-dependent chronic kidney disease (DD-CKD) patients or placebo in non-dialysis-dependent CKD patients (NDD-CKD). To earn an FDA nod, the data will need to demonstrate roxadustat’s MACE non-inferiority (no worse than) to both.
The company has stated that there are no “clinically meaningful differences” in MACE risk between roxadustat and EPO in DD-CKD and placebo in NDD-CKD but Plainview cites published data that showed large MACE and death imbalances, claiming that the company is keeping the negative results under wraps.
As far as pamrevlumab is concerned, Plainview is unconvinced that it has a role treating anything, doubting positive outcomes from late-stage studies in idiopathic pulmonary fibrosis (data readout in 2022) and locally advanced pancreatic cancer (readout in 2023), adding that the company is only conducting one trial in each so another study will be needed to support a U.S. marketing application for either indication, meaning potential approval is probably 9-10 years away.

Agile adds to Twirla-stoked rally, up 29%

Agile Therapeutics (AGRX +29.3%) is up on below-average volume on the heels of a positive Ad Com vote on contraceptive patch Twirla last week. Shares have rallied almost five-fold since then.
The FDA’s action date is Saturday, November 16, so a decision should be announced the day before.

Epizyme up 6% on funding deals

Epizyme (EPZM +6.3%) is up on below-average volume in reaction to its agreements with Royalty Pharma and its affiliate Pharmakon Advisors that, it says, could raise up to $270M in new capital, extending its cash runway into at least 2022.
The deal includes a $100M upfront investment by Royalty Pharma based on $15 per share and an 18-month option for Epizyme to sell an additional $50M of stock to Royalty at market prices not to exceed $20/share. Royalty has a three-year option to buy an additional 2.5M Epizyme shares at $20.
The parties have agreed to reduce the existing royalty rates owed by Epizyme to Royalty related to global sales of tazemetostat outside of Japan.
In a separate deal, Epizyme has established a $70M loan facility with Pharmakon which will fund the regulatory milestones owed to Eisai (OTCPK:ESALY +0.3%) triggered by NDA filings and approvals in the U.S. for epithelioid sarcoma and follicular lymphoma. It is expandable up to $300M following the FDA nod for follicular lymphoma, subject to mutual agreement.

NovaBay up 7% on online launch of CelleRx

NovaBay Pharmaceuticals (NBY +7.2%) perks up on below-average volume in response to the online launch of its CelleRx skin and wound cleanser.
The company says CelleRx is based on the same pure hypochlorous acid formulation as flagship product Avenova.

ICU Medical to acquire Pursuit Vascular

ICU Medical (ICUI -0.2%agrees to acquire Pursuit Vascular, a privately-held medical device company focused on catheter disinfecting products and technologies.
Deal is valued at $75M with an additional earnout payment potentially due in 2021.
Pursuit Vascular’s 2019 annual revenues are estimated to be ~$10M – $12M, with margins comparable to the existing ICU Medical IV consumables business.