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Friday, May 3, 2019

Acadia hopes for new indications for Nuplazid

Knockout interim data from Acadia’s trials of its antipsychotic in schizophrenia and dementia could make for early approval. But the chances of this are not high.
Acadia’s antipsychotic Nuplazid seems to have just about weathered the storm of safety concerns that sprang up around a year ago, with first-quarter 2019 sales of $63m, a jump of 29% year-on-year. Now Acadia’s attention is turning to expanding the indications for which Nuplazid may be used.
Nuplazid, a 5-HT2A inverse agonist currently approved for Parkinson’s disease psychosis, is in two crucial phase III trials both due to read out in the coming months. First up is the Enhance study in patients with an inadequate response to schizophrenia drugs, top-line data from which are expected mid-year.
The 380 patients in this study will take a background antipsychotic plus either Nuplazid – 10, 20 or 34mg per day, taken as two pills – or placebo. The primary endpoint is the change from baseline score on the positive and negative syndrome scale at six weeks. The company has said that approved schizophrenia drugs have shown an effect size of 0.25-0.5, so this could be a benchmark for approval, provided safety is clean.
The drug’s performance in phase II was mixed. In 423 patients with schizophrenia who had responded to earlier treatment, Nuplazid significantly enhanced the efficacy of Risperdal but actually lowered the efficacy of Haldol. At least safety was fairly benign, with no significant changes in treatment-emergent adverse events when Nuplazid was added to the other drugs.
If Nuplazid defies its phase II track record and scores a hit in Enhance, it probably stands a good chance of approval owing to the significant unmet need among patients who respond inadequately to other antipsychotics. Nothing is approved for this particular niche – it is separate to treatment-resistant schizophrenia, for which clozapine is approved.
But the risk that a confirmatory trial will be required even in the event that Enhance is a success is a sizeable one.
Hallucinations and delusions
Another schizophrenia study of Nuplazid, the phase II Advance in negative symptoms, ought to yield top-line data at the end of 2019. Before that, interim data from the phase III Harmony study in dementia-related psychosis will emerge.
Harmony is testing Nuplazid’s ability to prevent relapse in 356 patients with hallucinations and delusions associated with dementia-related psychosis. All patients were given 34mg of the drug for 12 weeks after which the non-responders were kicked off the trial. The responders were then randomly assigned to placebo or Nuplazid dosed at 20 or 34mg per day; the primary outcome is the time from randomisation to relapse in this latter, 26-week double-blind period.
According to Stifel analysts there is a slim chance that if positive, the interim data could be considered pivotal by the FDA. If the interim readout is not a total knockout Harmony will continue until its scheduled conclusion in 2020.
A look at Acadia’s pipeline, and the corresponding consensus forecasts compiled by EvaluatePharma, shows how enormously reliant on Nuplazid the company is. Schizophrenia is forecast to bring in $249m in 2024, though this primarily comes from the inadequate response indication, so a result in negative symptoms would be a boost.
Nuplazid’s use in dementia-related psychosis could add $267m to the group’s 2024 revenues. Acadia’s only other asset is the insulin-like growth factor 1 regulator trofinetide, which the sellside sees making just $57m in 2024 in the neurological condition Rett syndrome – peanuts compared with a forecast total of $1.7bn for Nuplazid.
ACADIA’S PIPELINE
   Annual WW indication sales ($m) 
ProductIndication Indication status20182020e2022e2024eIndication launch
NuplazidParkinson’s diseaseMarketed224453783950May 2016
NuplazidSchizophreniaPhase III15101249Dec 2020
NuplazidAlzheimer’s diseasePhase III11100267Dec 2020
NuplazidPsychosis, acutePhase III
NuplazidOther neurological indicationsPhase III
NuplazidDepressionPhase II41170Dec 2021
Trofinetide OralRett syndromePhase II857Dec 2022
Trofinetide OralFragile X syndromePhase II
Source: EvaluatePharma.

Amgen granted orphan status for lung cancer treatment

The FDA granted Amgen orphan status for its treatment of KRAS p.G12C-positive non-small cell lung cancer

Endo wins appeals court ruling upholding Opana ER patent

Bloomberg says

STAAR Surgical hit on FDA rejection of EVO marketing application

STAAR Surgical Company (STAA -20.9%) is down on modestly higher volume in early trade in reaction to its disclosure that the FDA has rejected its supplemental marketing application seeing approval for its EVO/EVO+ Visian Implantable Collamer Lens for myopia and EVO/EVO+ Visian Toric Implantable Collamer Lens for myopia with astigmatism.
The agency stated that the application was not complete enough to allow for review. Apparently, there were not enough data and analyses to prove safety and efficacy.
The company says it will continue its discussions with the regulator, including any new clinical data needed for a refiling.

Bristol-Myers upgraded to Overweight from Equal Weight at Barclays

Barclays analyst Geoffrey Meacham upgraded Bristol-Myers Squibb (BMY) to Overweight from Equal Weight and raised his price target for the shares to $55 from $53. The analyst says increased confidence in the Celgene (CELG) acquisition successfully closing makes him more bullish on Bristol-Myers shares. Increased optionality from the Celgene pipeline along with a “differentiated” growth profile and earnings power over the next few years make the combined company attractive at current share levels, Meacham tells investors in a research note.

Incyte downgraded to Equal Weight from Overweight at Barclays

Barclays analyst Geoffrey Meacham downgraded Incyte to Equal Weight from Overweight and lowered his price target for the shares to $82 from $90. With the stock up 27% year-to-date, the analyst does not see enough upside optionality from the company’s graft-versus-host disease opportunity or its early-stage pipeline.

Acceleron downgraded to Equal Weight from Overweight at Barclays

Barclays analyst Geoffrey Meacham downgraded Acceleron Pharma to Equal Weight from Overweight and lowered his price target for the shares to $45 from $54. Market expectations for luspatercept are now priced into the shares, leaving limited room for upside, Meacham tells investors in a research note.