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Fed Up with Washington, ALS Advocates Consider ACT UP's Take-No-Prisoners Approach

Next Wednesday, a cadre of ALS patients will gather for a protest outside the FDA’s headquarters in suburban Maryland with a clear message: “No More Excuses.”

The rally is being organized by a ragtag group of ALS patients who connected mostly through Facebook, and it’s far less a production than other efforts like the 2014 ice bucket challenge that swept around the world.

These protesters haven’t even established a formal organization or a website; some said they’ve never even been to a protest. There’s nary a poster board in sight, yet.

But the band of patients is already catching the attention of regulators at the Food and Drug Administration, establishment advocates at the ALS Association, and top bioethicists around the country. Top Senate lawmakers, too, are beginning to advocate for their cause.

These protesters say, at least, that they plan to emulate the aggressive, even “radical” approaches and the take-no-prisoners strategy of the AIDS activists who protested the FDA’s slow work on that disease in the 1980s. Like the ACT UP activists before them, the ALS patients are coming armed with a list of specific therapies they want regulators to approve—and fast. But unlike their predecessors, they’re hoping not to be arrested next week.

The ALS patients are fed up: They had hoped that the $115 million raised from the viral ice bucket challenge would be poured into promising research. They’ve seen no results from their advocacy for the national “right-to-try” law that promised access to new cures. And they’ve felt left out as the FDA approved treatments for other similarly fatal neuromuscular diseases.

“We as ALS patients are just tired of no action being taken on our part,” said Mike Henson, one of the organizers. “I don’t know what’s worse, getting ALS 10 years ago and just knowing you’re going to die or getting it now and knowing that you could be saved if only people would take this seriously.”

Henson lives in Tulsa, Okla., and was diagnosed with ALS last year. He is a former logistics manager for a rock casino who speaks his mind, calling ALS “a murderous son of a bitch of a disease.’’ He’s made a name for himself in the ALS community by starting his own ALS talk show on YouTube, complete with a chyron and green screen.

Just Wednesday, the protesters adopted a name for their troupe: “Contagious for A Cure.”

And there’s a specific potential cure they’re seeking—or rather, for now, there are three. A trio of drug companies is in the middle of the development process for separate, still-investigational ALS drugs: BrainStorm’s stem cell treatment NurOwn, Collaborative Medicinal Development’s synthetic molecule CuATSM, and Dr. Stanley Appel’s cell therapy known as Tregs.

The drugs are all at quite different stages of clinical development: BrainStorm is currently enrolling a Phase 3 clinical trial, Collaborative Medicinal Development has only completed Phase 1 testing, and Appel’s Tregs has only been studied in three patients.

For those knowledgeable about ALS, it feels like deja vu: ALS patients have demanded access to BrainStorm’s NurOwn throughout the fight for a federal right-to-try law. So much so that the company’s CEO Chaim Lebovits promised that patients would be able to access the drug once right to try was law, only to largely go back on that promise and instead provide access to only one right-to-try activist, Matt Bellina. (BrainStorm declined to comment for this story.)

Henson and his fellow organizers want to know why these drugs aren’t being fast-tracked through the FDA’s approval process, especially while drugs for other neuromuscular diseases are being approved, seemingly left and right. He points to Zolgensma, Novartis’ gene therapy for spinal muscular atrophy, which was approvedbased on a trial of only 15 children—albeit with impressive results.

“That drug was approved very quickly with a very small trial,” Henson said. “So, we know this can be done, if we have the will to do this.”

The FDA said it “stands ready to help” the ALS community—including by helping patients and their doctors evaluate options like clinical trials or using the FDA’s expanded access program to get ahold of experimental, unapproved treatments. A spokeswoman also said the agency “is prepared to use all expedited development and approval programs at its disposal” to make new treatments available.

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Two top officials in the agency’s drug approval centers, Janet Woodcock and Peter Marks, also offered to meet with advocates and drug makers, so long as the drug makers would also participate.

“We encourage you to reach out to each of the manufacturers to request a meeting with the agency that includes you and any other members of the ALS community that you would like to include. With their permission, we welcome the opportunity to have a transparency discussion about their investigational products,” Woodcock and Marks wrote in an email shared with STAT.

More and more, cries for more progress are coming from Capitol Hill as well. Republican Sens. Ted Cruz (Texas), Marco Rubio (Fla.), Mike Braun (Ind.) and Mike Lee (Utah) wrote to acting FDA Commissioner Ned Sharpless last month making a similar demand.

The senators are calling for the FDA to bring back the so-called parallel track that the agency unveiled for AIDS patients in the 1990s. Under that pathway, which was never extended beyond HIV and AIDS patients, those ineligible for clinical trials could gain access to certain drugs still being studied. It’s estimated that thousands of AIDS patients got access to one such drug, Stavudine, under the parallel track in the 1990s.

“It is time for the FDA to create and encourage an environment that promotes patient choice, patient access, and patient affordability,” they wrote. “Expansion of the Parallel Track is a proven solution to do just that, and we strongly encourage the FDA to act immediately on this issue.”

It’s a perplexing request. In the years since it created the parallel track, the FDA has stood up several more concrete pathways for patients to access experimental drugs.

The FDA isn’t the only target of these protesters. The group also plans to protest the ALSA. They want answers as to why the $115 million raised by the ice bucket challenge hasn’t gone to fund development of their three favorite potential therapies. ALSA has technically funded two of the therapies, although the protestors insist their funding was not nearly enough.

“What we just can’t figure out is why ALSA is not vigorously pursuing getting any of these drugs into our bodies immediately!” the organizers of next week’s protest wrote to ALSA.

They’re so frustrated with ALSA that they’re calling for the resignation of the group’s President and CEO Calaneet Balas.

In a statement to STAT, ALSA said it was “working urgently to end ALS,” which includes funding “many early stage clinical trials and work[ing] with the FDA and scientists to help trials run faster.” An ALSA-sponsored report released Tuesday also found that the ice bucket challenge resulted in ALSA increasing its research funding by 187%. Among the achievements from that research: discovery of five new genes potentially tied to ALS.

But the protestors want more specific commitments from ALSA to work with BrainStorm, Appel, and Collaborative Medicinal Development “with the ultimate goal of having any of these viable therapies available to the ALS community within the next 6 months maximum.”

Henson is convinced these three treatments—either alone or in some combination—are the cure to curing ALS.

“They’ve been proven,” he insisted.

Republished with permission from STAT. This article originally appeared on June 7, 2019

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