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Monday, November 22, 2021

Mirati, Verastem to Evaluate Combo in Non-Small Cell Lung Cancer

 Mirati Therapeutics, Inc. (Nasdaq:MRTX), a clinical-stage targeted oncology company and Verastem Oncology (Nasdaq:VSTM), a biopharmaceutical company committed to advancing new medicines for patients battling cancer, today announced a non-exclusive clinical collaboration agreement to evaluate the combination of Mirati's investigational KRASG12C inhibitor adagrasib with Verastem Oncology's investigational RAF/MEK inhibitor VS-6766 in KRASG12C-mutant non-small cell lung cancer (NSCLC).

The primary objective of this multi-center, single-arm, open-label Phase 1/2 trial is to determine the maximum tolerated dose and recommended Phase 2 dose for the combination of adagrasib and VS-6766 in patients with KRASG12C-mutant NSCLC. The study will also investigate the safety, tolerability and efficacy of the combination in patients who have progressed on a KRASG12C inhibitor. The trial will build on preclinical data showing deeper blockade of ERK pathway signaling resulting in enhanced anti-tumor efficacy with the combination of adagrasib and VS-6766 relative to either agent alone.

https://finance.yahoo.com/news/mirati-therapeutics-verastem-oncology-partner-123000376.html

Pfizer's COVID-19 vaccine trial data shows long-term efficacy in adolescents

 Pfizer Inc said on Monday its COVID-19 vaccine provided strong long-term protection against the virus in a late-stage study conducted among adolescents aged 12 to 15 years.

A two-dose series of the vaccine was 100% effective against COVID-19, measured seven days through over four months after the second dose, the company said.

The long-term data will support planned submissions for full-regulatory approval of the vaccine in the age group in the United States and worldwide.

Pfizer and BioNTech will seek clearance for a 30 micrograms dose of the vaccine for those aged 12 and above.

The vaccine was authorized for emergency use in people aged 12-15 years by the U.S. Food & Drug Administration in May, and granted full approval for use in people aged 16 and above in August

https://finance.yahoo.com/news/1-pfizers-covid-19-vaccine-121700171.html

Neurocrine started at Underperform by BMO

 Target $76

https://finviz.com/quote.ashx?t=nbix&ty=c&ta=1&p=d

Royalty Pharma Acquires Additional Royalty Interests in BCX9930 and ORLADEYO from BioCryst

 Royalty Pharma plc (Nasdaq: RPRX), BioCryst Pharmaceuticals, Inc. (Nasdaq: BCRX) and OMERS Capital Markets (OMERS) today announced transactions totaling $350 million in new funding for BioCryst, with all funds immediately available at closing.

The funds from these transactions will enable further advancement of BCX9930, BioCryst’s oral Factor D inhibitor, toward filing for registration, expand the development of BCX9930 across multiple indications and support additional investment in the global launch of ORLADEYO® (berotralstat), which is on a trajectory to become the market-leading prophylactic hereditary angioedema (HAE) therapy.

For a $150 million upfront cash payment, Royalty Pharma, the largest buyer of pharmaceutical royalties globally, has purchased royalties on combined annual net sales of BCX9930 and another earlier stage Factor D inhibitor of 3.0% on sales up to $1.5 billion, 2.0% on sales between $1.5 billion and $3.0 billion, and no royalty on sales over $3.0 billion. Royalty Pharma also purchased royalties of 0.75% on direct annual net sales of ORLADEYO up to $350 million, 1.75% on sales between $350 million and $550 million, no royalty on sales over $550 million, and a tiered, declining percentage on ORLADEYO sublicense revenue in certain territories. These royalties are additional to the royalties purchased by Royalty Pharma in December 2020.

For a $150 million upfront cash payment, OMERS, one of Canada’s largest defined benefit pension plans, has purchased a capped, tiered, declining royalty on direct annual net sales of ORLADEYO. Under the agreement, BioCryst does not owe any royalties for the first two years. The first royalty payment from BioCryst to OMERS will occur based on royalties from direct annual net sales of ORLADEYO in the fourth quarter of 2023. Once OMERS has achieved its maximum allowed total return under the agreement, no further royalty payments will be owed. OMERS will receive a royalty of at least 7.5% on annual net sales up to $350 million, 6.0% on sales between $350 million and $550 million and no royalty on sales over $550 million. The maximum total return OMERS may earn under the agreement is capped at 1.425x or 1.550x, based on the level of 2023 global net sales of ORLADEYO relative to a prespecified sales threshold.


REGENXBIO Gets Orphan Drug Tag for Duchenne Gene Therapy Candidate

 

  • Potential one-time gene therapy for the treatment of Duchenne, includes a novel, optimized microdystrophin transgene and REGENXBIO's proprietary NAV® AAV8 vector

  • Commercial-scale cGMP material to be used in clinical development

  • Company on track to submit IND by end of 2021

REGENXBIO Inc. (Nasdaq: RGNX) today announced the U.S. Food and Drug Administration (FDA) granted Orphan Drug Designation for RGX-202, a potential one-time gene therapy for the treatment of Duchenne muscular dystrophy (Duchenne). RGX-202 is designed to deliver a novel, optimized microdystrophin transgene with a unique C-terminal domain and a muscle specific promoter to support targeted therapy for improved resistance to muscle damage associated with Duchenne. RGX-202 uses REGENXBIO's proprietary NAV® AAV8 vector.

https://finance.yahoo.com/news/regenxbio-announces-orphan-drug-designation-120000054.html

Proventtion: Regulatory Update for Teplizumab At-Risk Type 1 Diabetes Approval Path

 Provention Bio, Inc. (Nasdaq: PRVB), a biopharmaceutical company dedicated to intercepting and preventing immune-mediated disease, today provided an update on its ongoing efforts to address U.S. Food and Drug Administration (FDA) considerations cited in the Complete Response Letter (CRL) issued to the Company by the FDA on July 2, 2021, pertaining to comparability between the Company's planned teplizumab commercial product and clinical drug product used in historical trials of teplizumab.

On November 18, 2021, the Company had a Type A meeting with the FDA to discuss the population pharmacokinetic (popPK) model to be used for the purpose of planned commercial and clinical drug product comparison. In preliminary meeting comments, the FDA approved the Company proceeding to populate the popPK model with data collected from patients receiving therapeutic doses of teplizumab in a pharmacokinetic/pharmacodynamic (PK/PD) substudy of the ongoing PROTECT Phase 3 trial in newly diagnosed type 1 diabetes (T1D) patients (Commercial Product N~30 patients, Clinical Drug Product N~130 patients).

The Company's preliminary analysis from the popPK model produced the following top-line results:

Geometric mean of the ratio of commercial to clinical drug product [90% Confidence Interval (CI)]

  • 83.2% AUC Infinity [CI: 76.9 – 89.9]

  • 85.3% AUC Day 13 [CI: 78.0 – 93.3]

  • 86.5% CMAX [CI: 83.9 – 89.3]

These results are not final and are subject to ongoing review of both the data and the popPK model by the FDA and the Company.

As anticipated, given teplizumab's target mediated mechanism of clearance, the difference in exposure (AUC Day 13 and 0-infinity) between commercial product and clinical drug product observed in a prior single, fractional low dose PK/PD study in healthy volunteers is greatly reduced when the products are administered and compared in accordance with the higher therapeutic dosing regimen used in T1D patients. Along with previously reported physicochemical and pharmacodynamic data, as well as the immunogenicity and safety profiles, it is the Company's current opinion that, collectively, these preliminary results support comparability of the commercial product and clinical drug product. The FDA, the ultimate decision maker on the matter, is conducting an independent review of the data and may have a different opinion. The Company looks forward to further discussing these results with the FDA to support the FDA's review.

Sunday, November 21, 2021

Japan sees 'drug lag' as foreign pharmas pass up market amid pricing pressure

 Japan has been leveraging different policy tools to rein in drug expenditures, and that is scaring foreign pharmas away.

The country is seeing “trends of a drug lag,” as approvals decrease, Yasushi Okada, president of the Japan Pharmaceutical Manufacturers Association and Eisai’s chief operating officer, said in a recent interview, as quoted by local news agency Jiji Press.

Altogether, 176 new drugs that were approved in the U.S. and Europe between 2016 and 2020 didn’t enter Japan, up from 117 in the five years leading up to 2016, according to the industry group.

“An industry will not prosper unless technological innovation is rewarded,” Okada said, as quoted by Jiji. “We barely feel any advantage from being based in Japan.”

Okada’s comment comes as Japan this year reportedly implemented its first “off-year” price cut outside of its planned biennial drug price revisions. Japan adjusts drug prices biennially mainly to close the gap between the reimbursement price and the actual purchase price on the market.

Okada, in particular, took issue with how Japan slashes drug prices simply when sales exceed certain thresholds. The country maintains a system of repricing for market expansion, which pares back prices when annual sales vastly exceed a drug’s original estimated figure. In extreme cases, authorities may cut a maximum of 25% off a drug’s price if its annual sales rise to between 100 billion yen and 150 billion yen and are at least 1.5 times the original expected sales or 50% off when sales exceed 150 billion yen.

The most well-known case that experienced a price cut under this scheme was perhaps Ono Pharmaceutical’s Opdivo, which was licensed to Bristol Myers Squibb outside of Japan.

Opdivo originally launched in Japan in 2014 in the small indication of melanoma. But its sales growth from label expansions to such areas as non-small cell lung cancer spooked Japanese authorities, which singled out the drug in a special repricing with a hefty 50% discount, which took effect in 2017. The PD-1 inhibitor went on to take several more rounds of price cuts in the following years.

The repricing for market expansion rule is just one of several tools the Japanese government has resorted to for cutting drug prices. This year, Japan started officially applying a cost-effectiveness assessment (CEA) system to drug prices, two years after its introduction in April 2019. Novartis’ CAR-T therapy Kymriah and GlaxoSmithKline’s three-in-one COPD inhaler Trelegy became the first two treatments to undergo an assessment under the program. Starting in July, those drugs will see a 4.3% and 0.5% price cut, respectively.

Gilead Sciences’ rival CAR-T drug, Yescarta, which is managed by Daiichi Sankyo in Japan, got the same 4.3% downward adjustment from the get-go because its original reimbursement price was benchmarked against Kymriah. Back in 2019, Kymriah won Japanese coverage at a price of 33.5 million yen, whereas Yescarta secured approval earlier this year.

The CEA system, which uses an incremental cost-effectiveness ratio for its calculations, targets highly innovative but pricey drugs.

Okada also opposes a proposal to tie the maximum increase in drug prices to the growth rate of Japan’s nominal GDP, according to Jiji. “The pharmaceutical industry has the potential to make money,” he said. “It must lead GDP growth instead.”

https://www.fiercepharma.com/pharma-asia/japan-sees-drug-lag-as-foreign-pharmas-skip-market-amid-pricing-pressure-industry-group