ANA 2021 – Ionis rocked by tofersen flop

 The amyotrophic lateral sclerosis field has had more than its fair share of disappointments. The latest one came yesterday, with the failure of Biogen and Ionis’s Sod1-targeted project tofersen in the phase 3 Valor study.

Bulls are clinging to a decrease seen in a biomarker of axonal damage, neurofilament light chain, with some believing that this could pave the way to an accelerated approval. Even sellside analysts poured cold water on this idea, but the companies do have another shot with an ongoing trial in presymptomatic ALS.

For now, though, tofersen’s future looks dim. This might not be such a big deal for Biogen: Sod1 mutations only account for around 2% of ALS patients, and the market for tofersen was always expected to be small. The group’s stock sank just 1% this morning.

It is a bigger blow for Ionis and its antisense approach more broadly, especially after the failure of the Roche-partnered Huntington’s project tominersen earlier this year. Ionis’s stock was down as much as 12% this morning.

The better part of Valor

The data from Valor, presented at the American Neurological Association meeting, raised many questions, but there is no doubt that the study failed. It did not meet the primary endpoint, change in the revised amyotrophic lateral sclerosis functional rating scale (ALSFRS-R) at 28 weeks versus placebo.

There was no benefit on ALSFRS-R in either subgroup studied: those with fast-progressing disease – the primary analysis population – or slowly-progressing ALS.

Source: Biogen presentation & ANA 2021

However, some believe there are glimmers of hope to be found. For a start, tofersen did what it was designed to do: decrease levels of Sod1. In patients with this mutation, aberrant Sod1 protein is prone to misfolding, resulting in toxicity; the theory was that hitting this protein could slow disease progression.

One question now is why, in the case of tofersen, this did not lead to an improvement in function. Stifel analysts noted that the magnitude of Sod1-lowering, at 30-40%, was only “moderate” and added that the short trial duration might provide another possible explanation for the failure.

Bulls were also encouraged by a 50-60% reduction in neurofilament light chain (NfL) in tofersen-treated patients. This suggests that the project could be slowing neurodegeneration; it is notable that some multiple sclerosis drugs are associated with decreases in NfL.

However, even Stifel, self-proclaimed “believers” in NfL as a surrogate biomarker in neurology, questioned whether the NfL result would be enough for approval, particularly given the clear miss on Valor’s primary endpoint.  

Leerink agreed, writing: “We don’t see how Biogen would be able to proceed with a filing with this data.” Biogen itself has not disclosed its plans, but said it was “actively engaging with regulators” to determine the next steps.

Adverse events could give the likes of the FDA pause: there were four severe neurological events in the tofersen arm, including two cases of myelitis, versus no such events in the placebo cohort. However, in a disease like ALS, this level of risk would probably be acceptable.

Earlier the better?

The lack of efficacy is concerning, but it is possible that earlier therapy is needed. As with many neurological diseases, protein aggregates can form well before the onset of symptoms.

Biogen and Ionis are already testing this theory in the Atlas trial, which is enrolling presymptomatic subjects with Sod1 mutations and elevated levels of NfL. The primary endpoint is the proportion of participants with emergence of clinically manifest ALS within 12 months of randomisation, but data might be a while – according to clinicaltrials.gov, the study is set to complete in 2026.

Ionis and Biogen have other genetically targeted neurology projects in the works, but today's investor disappointment suggests that hopes might have dimmed for these approaches more broadly. In ALS the companies are partnered on BIIB078, a phase 1 project aimed at a genetic form of the disease, C9orf72-associated ALS, and they are developing various genetically targeted agents in the CNS space more broadly. Ionis also has a wholly-owned phase 3 asset, ION363, designed for those with mutations in the FUS gene.

A recent analysis by Evaluate Vantage found plenty of mid-to-late-stage assets in development for ALS, as the table below shows. But Biogen and Ionis just reminded investors that getting a result in this disease is easier said than done.

Selected ALS projects in mid-to-late-stage clinical development
Project	Mechanism	Company	Trial details/note
Phase 3
Tofersen	Sod1 antisense oligo	Biogen/Ionis	Valor in symptomatic pts failed Oct 2021; Atlas in presymptomatic subjects ends Aug 2026
Alsitek (masitinib)	CD117, FGFR3 & PDGFR antagonist	AB Science	AB19001 ends Dec 2022
Reldesemtiv	Troponin activator	Cytokinetics	Courage-ALS ends Dec 2023; project previously failed in ALS
Jacifusen (ION363)	Fused in sarcoma antisense	Ionis	NCT04768972 ends Mar 2024
AMX0035 (sodium phenylbutyrate + Taurursodiol)	Histone deacetylase inhibitor + bax inhibitor	Amylyx	Phoenix not yet recruiting; Amylyx plans filing based on ph2 Centaur data
Phase 2/3
CuATSM	Copper-containing synthetic small molecule	Collaborative Medicinal Development	NCT04082832 primary completion date Dec 2020 but still recruiting
Zilucoplan	Complement factor C5 inhibitor	UCB	HEALEY ALS Platform Trial – Regimen A* ends Oct 2021
Verdiperstat	Myeloperoxidase enzyme inhibitor	Biohaven	HEALEY ALS Platform Trial – Regimen B* ends Oct 2021
CNM-Au8	Elemental gold nanocrystals	Clene Nanomedicine	HEALEY ALS Platform Trial – Regimen C* ends Oct 2021; ph2 Rescue-ALS data due Q4'21
Pridopidine	Sigma-1 receptor agonist	Prilenia	HEALEY ALS Platform Trial – Regimen D* ends Mar 2022
MN-166 (ibudilast/Ketas)	Phosphodiesterase inhibitor	Medicinova	Combat-ALS ends Dec 2023
Phase 2
PrimeC (ciprofloxacin + celecoxib)	Antibiotic/Cox-2 inhibitor & NSAID	Neurosense Therapeutics	NCT04165850 ended Jan 2021
ALZT-OP1a (cromolyn + ibuprofen)	Mast-cell stabiliser/NSAID	Aztherapies	NCT04428775 ended Jul 2021
RT001	Synthetic omega-6 fatty acid	Retrotope	NCT04762589 ended Sep 2021
ANX005	Anti-complement factor C1q MAb	Annexon Biosciences	NCT04569435 data due 2022
3K3A-APC	Activated protein C analogue	ZZ Biotech	NCT05039268* ends Jan 2022
AT-1501	Anti-CD40L MAb	Eledon Pharmaceuticals	NCT04322149 ends Mar 2022
BLZ945	CSF-1 inhibitor	Novartis	NCT04066244 ends Apr 2022 (prev Sep 2021)
Empaveli	Complement factor C3 inhibitor	Apellis	Meridian ends Sep 2022
Engensis	HGF gene therapy	Helixmith	Revivals-1A ends Dec 2022
SNR1611	Mek inhibitor	Genuv	Ph1/2 (NCT04326283) ends Dec 2022
PU-AD	Heat shock protein 90 inhibitor	Samus Therapeutics	NCT04505358 ends Dec 2022 (prev Dec 2021)
WVE-004	C9orf72 antisense oligo	Wave Life Sciences	Ph1/2 Focus-C9, also includes pts with FTD; ends Feb 2023
AL001	Sortilin inhibitor	Alector/Glaxo	NCT05053035, ends Feb 2023
RNS60	Oxygen nanobubbles	Revalesio	NCT02988297 (nebulised version), ends Dec 2023
Q-Cells	Human glial restricted progenitor cells	Q Therapeutics	Ph1/2 (NCT02478450) ends Dec 2023
*Investigator-sponsored study. Source: Evaluate Pharma & clinicaltrials.gov. https://www.evaluate.com/vantage/articles/news/trial-results/ana-2021-ionis-rocked-tofersen-flop

Avadel delay hands Jazz another narcolepsy boost

 A delay to the FDA’s decision on Avadel’s narcolepsy project, FT218, allows Jazz investors a second bout of schadenfreude in as many weeks. The once-a-night pill could become a big competitor to Jazz’s twice-a-night Xyrem/Xyway franchise; the news follows the exit of another potential rival, Takeda’s TAK-994, recently abandoned on safety concerns. When the FDA’s verdict on FT218, which had a Pdufa date of October 15, might emerge is unclear. Avadel insists the regulator made no new information requests, saying only that action was unlikely in October. A short delay due to a lack of resources at the agency would be the best case scenario. However, the FDA could be mulling more serious issues, Stifel analysts mooted: firstly that Avadel might need to go down the generic filing route – Xyrem/Xyway and FT218 contain the same active ingredient – a scenario that would lead to a 30-month stay to approval. Or perhaps the agency is considering whether FT218 really deserves orphan drug exclusivity, which is largely based on its dosage advantage. A 15% drop in Avadel’s stock this morning suggests investors are cautiously optimistic that the delay will be short. The outlook for the narcolespy market, below, shows what is in play. 

 Xyrem - Jazz: $1 336m

https://www.evaluate.com/vantage/articles/news/snippets/avadel-delay-hands-jazz-another-narcolepsy-boost

EPA to regulate certain 'forever chemicals' in drinking water in 2023

 The EPA on Monday released its strategy for addressing a type of cancer-linked chemicals called PFAS, including its plans to finish a rule to regulate certain types of PFAS in drinking water in 2023.

PFAS stands for perfluoroalkyl and polyfluoroalkyl substances, and these substances are a group of man-made chemicals that have been linked to health problems such as kidney and testicular cancer.

According to the Centers for Disease Control and Prevention, exposure rates can be difficult to assess, but one 2015 study found PFAS to be in the blood of 97 percent of Americans.

The EPA’s overall strategy is focused on researching PFAS, restricting its release into the air, land and water and broadening cleanup efforts. 

The agency’s drinking water limit pertains to certain types of PFAS called PFOA and PFOS, saying it hopes to propose an enforceable drinking water limit for them in fall 2022 and finalize it in fall 2023. 

The Trump administration also eyed regulating PFOA and PFOS, proposing its own regulation on the substances last year.  

The drinking water standard is a long-awaited milestone for environmental advocates, but some have called for PFAS to be regulated as an entire group instead of on an individual basis because there are hundreds of them and they can occur in mixtures. 

The EPA is also developing a new testing strategy for the substances. 

As part of that strategy, the agency is expected to require manufacturers to conduct and fund studies, and could issue testing orders by the end of this year.  

The agency has also said that it will declare PFOA and PFOS as hazardous substances under the country’s Superfund hazardous waste cleanup law.  

This would require polluters to report discharges of the compounds and give the EPA the ability to recoup costs for their cleanup.  

The EPA will propose a regulation to do so in spring 2022 and finalize the decision in summer 2023. The Trump administration had also floated a hazardous substance designation for the two chemicals. 

The agency has previously announced that it would set discharge limits for certain industries. The push was highlighted in the roadmap, saying such rules would apply to the organic chemicals, plastics and synthetic fibers, metal finishing and electroplating industries. 

It also said it would launch detailed studies for other industries including for landfills, textile mills and electrical components.  

The agency also said that it plans to publish additional assessments on the toxicity of other types of PFAS starting this fall. These assessments can be used to issue health advisories.  

Two of the chemicals it will publish these assessments for are known as “GenX chemicals,” which have been found in water and air, including in North Carolina’s Cape Fear River. 

A fact sheet from the White House also highlighted actions being taken by other agencies.  

That memo said the Defense Department is conducting cleanup assessments at 700 installations. Meanwhile, the Food and Drug Administration will expand its food testing and the Agriculture Department is supporting research on PFAS in the food system. 

The Hill reported this month that the agency’s roadmap was coming soon and obtained slides showing that it was aiming to address “inadequate” regulations, “disproportionate impacts on vulnerable groups” and “the need for prevention” for PFAS that get into the environment

EPA administrator Michael Regan categorized the plan as a “comprehensive” strategy to protect people. 

“For far too long, families across America — especially those in underserved communities — have suffered from PFAS in their water, their air, or in the land their children play on,” he said in a statement.

“This comprehensive, national PFAS strategy will deliver protections to people who are hurting, by advancing bold and concrete actions that address the full lifecycle of these chemicals. Let there be no doubt that EPA is listening, we have your back, and we are laser focused on protecting people from pollution and holding polluters accountable,” he added.

https://thehill.com/policy/energy-environment/577158-epa-to-regulate-certain-types-of-forever-chemicals-in-drinking

Infinity Pharma started at Buy by Wainwright

 Target $9

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

Progenity started at Buy by Wainwright

Target $4

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Omeros Gets Complete Response Letter for Biologics License Application

 Omeros Corporation (Nasdaq: OMER) today announced that the company received a Complete Response Letter (CRL) from the U.S. Food and Drug Administration (FDA) regarding its Biologics License Application (BLA) for narsoplimab in the treatment of hematopoietic stem cell transplant-associated thrombotic microangiopathy (HSCT-TMA).

Following HSCT, patients generally have complex clinical courses and are often severely ill. HSCT-TMA increases that complexity and worsens outcomes. In the CRL, FDA expressed difficulty in estimating the treatment effect of narsoplimab in HSCT-TMA and asserted that additional information will be needed to support regulatory approval. There were no chemistry, manufacturing and controls (CMC), safety, or non-clinical issues precluding approval raised in the CRL.

Omeros remains confident in the efficacy and safety data for narsoplimab in HSCT-TMA. The company worked closely with FDA on the clinical development plan, including with respect to both the single-arm trial to support approval and the definition of response as the primary endpoint.

Omeros plans to request a Type A meeting as soon as possible with FDA to discuss the CRL and determine the most expeditious path forward for the approval of narsoplimab in the treatment of HSCT-TMA.

Narsoplimab is the first drug candidate submitted to FDA for approval in HSCT-TMA. It has Breakthrough Therapy and Orphan designations in both HSCT-TMA and IgA nephropathy.

Conference Call Details

Omeros’ management will host a conference call to discuss today’s announcement. The call will be held today at 8:30 a.m. Eastern Time; 5:30 a.m. Pacific Time. To access the live conference call via phone, please dial (844) 831-4029 from the United States and Canada or (920) 663-6278 internationally. The participant passcode is 9549686. A telephone replay will be available for one week following the call and may be accessed by dialing (855) 859-2056 from the United States and Canada or (404) 537-3406 internationally. The replay passcode is 9549686.

https://finance.yahoo.com/news/omeros-receives-complete-response-letter-103000914.html

PTC Therapeutics cut to Underperform from Neutral by B of A

 Target $38

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