Placebo

Spiral Therapeutics Announces Collaboration with the Vestibular Disorders Association (VeDA), Advancing Patient-Centric Care in Neurotology

Retrieved on: 
Tuesday, October 31, 2023

This alliance aims to improve the lives of patients suffering from balance disorders like Meniere's Disease through targeted outreach, collaborative patient education programs, and data-driven research.

Key Points: 
  • This alliance aims to improve the lives of patients suffering from balance disorders like Meniere's Disease through targeted outreach, collaborative patient education programs, and data-driven research.
  • "Joining forces with VeDA is a significant milestone for Spiral, as it aligns with our commitment to address the unmet medical needs in the field of inner ear disorders," said Hugo Peris, CEO of Spiral Therapeutics.
  • This collaboration grants Spiral access to VeDA's Patient Registry on Meniere's patients, enriching its ongoing research efforts.
  • Encouraged by these milestones, Spiral plans to submit an Investigational New Drug (IND) application for SPT-2101 in the United States in 2024.

FDA advisory panel's conclusion that oral phenylephrine is ineffective means consumers need to think twice when buying cold and flu meds

Retrieved on: 
Thursday, October 26, 2023

The ramp-up to cold and flu season is a bad time for consumers to learn that some of their most trusted go-to products don’t actually work.

Key Points: 
  • The ramp-up to cold and flu season is a bad time for consumers to learn that some of their most trusted go-to products don’t actually work.
  • The 2023 FDA advisory panel met to review growing evidence that oral phenylephrine is an ineffective treatment for nasal congestion.
  • Consumers may also question whether combination cough, cold and flu products will still be safe and effective for use at home.

The backstory

  • The most recent analysis is not the first time an FDA advisory panel has scrutinized oral phenylephrine.
  • A 2007 panel examining its use concluded that more studies were needed to make a final decision regarding the effectiveness of phenylephrine.

Safety concerns

  • No safety issues with oral phenylephrine alone were documented in the 2023 advisory panel conclusion.
  • However, researchers and advisory panel members have raised concerns about the possibility of products containing ineffective phenylephrine remaining on pharmacy shelves.
  • Even if oral phenylephrine is safe, taking an ineffective medication could cause consumers to spend money on products that work no better than a placebo.

The story behind pseudoephedrine

  • Luckily, the nonprescription oral nasal decongestant pseudoephedrine – which is known to be effective – has been commercially available for many years.
  • Pseudoephedrine is a nasal decongestant that is taken by mouth to relieve a stuffy nose.
  • If the FDA acts on the advisory committee’s conclusions that oral phenylephrine is not an effective nasal decongestant, pseudoephedrine may be the only remaining oral medication available without a prescription to treat nasal congestion.


Pseudoephedrine should not be used in doses higher than those that are recommended on the label. Use of products containing pseudoephedrine should be stopped and a health care provider consulted if dizziness, nervousness or sleeplessness occurs.
Pseudoephedrine should not be used by consumers with heart disease, high blood pressure, thyroid disease, diabetes or an enlarged prostate without talking with a health care provider like a pharmacist or a physician.
Products with pseudoephedrine should not be used while taking, or within two weeks of stopping, a prescription monoamine oxidase inhibitor, which is most commonly used to treat for depression or Parkinson’s disease.

Other treatments

  • These products are sold under the brand name Afrin and others.
  • All of these non-drug approaches can help sooth the nasal passage to provide temporary relief from congestion.
  • If symptoms of congestion continue for more than two weeks, or if signs of an infection arise, go see your doctor.


Lucas Berenbrok is part owner of the consulting company, Embarx, LLC. Colleen Culley and Karen Steinmetz Pater do not work for, consult, own shares in or receive funding from any company or organization that would benefit from this article, and have disclosed no relevant affiliations beyond their academic appointment.

Inhibikase Therapeutics Highlights Unblinded Functional Analysis from the 201 Trial of Risvodetinib in Untreated Parkinson’s Disease and Provides Update on Ongoing Enrollment

Retrieved on: 
Monday, October 16, 2023

These participants were withdrawn from the trial following the FDA’s temporary clinical hold in November, 2022 that was lifted in January, 2023.

Key Points: 
  • These participants were withdrawn from the trial following the FDA’s temporary clinical hold in November, 2022 that was lifted in January, 2023.
  • The Company also provided an update on the enrollment progress and recruitment tools being used in the ongoing 201 Trial.
  • In August 2023, Inhibikase presented an analysis of the primary and secondary endpoints performed on these eleven participants at the Movement Disorders Society Congress.
  • The Company also detailed changes in the functional assessments of motor and non-motor features using a hierarchical analysis of fifteen secondary endpoints.

Omeros Corporation Provides Update on Interim Analysis of ARTEMIS-IGAN Phase 3 Trial of Narsoplimab in IgA Nephropathy

Retrieved on: 
Monday, October 16, 2023

Topline results show that narsoplimab did not achieve statistically significant improvement over placebo.

Key Points: 
  • Topline results show that narsoplimab did not achieve statistically significant improvement over placebo.
  • The UPE reduction in the placebo group was markedly greater than that reported in trials of other agents in IgA nephropathy.
  • Based on the absence of statistical significance and as previously agreed with FDA, Omeros will not submit an application for approval of narsoplimab in this indication and will discontinue the ARTEMIS-IGAN clinical trial.
  • “We want to thank all the patients and investigators who participated in the trial,” said Gregory A. Demopulos, M.D, chairman and chief executive officer of Omeros.

Hemp, Inc.’s Creative Visionary Consultant, Bruce Perlowin, to be Interviewed Live on the Quantum Energy, Health, and Information Call Today

Retrieved on: 
Monday, September 18, 2023

Tune in to gain valuable insights on how Hemp, Inc.’s CBD health and wellness product line can be an asset to your daily health routine.

Key Points: 
  • Tune in to gain valuable insights on how Hemp, Inc.’s CBD health and wellness product line can be an asset to your daily health routine.
  • There’s a stark contrast between our highly potent, highly absorbable CBD product and most other products on the market."
  • Perlowin’s sentiments underscored the remarkable quality and potency of Hemp, Inc.'s CBD offerings and emphasized the company's commitment to delivering premium, effective CBD solutions to consumers.
  • Hemp, Inc.’s analysis of published clinical trials showed that entry-level results began around 150 milligrams of CBD and 50 milligrams of CBG.

LIB Therapeutics and Hasten Biopharmaceutical Company Announce $325 Million Strategic Collaboration to Develop and Commercialize Lerodalcibep in Greater China

Retrieved on: 
Tuesday, September 12, 2023

LIB Therapeutics Inc. (“LIB”) and Hasten Biopharmaceutical Co., Ltd. (“Hasten”), today announce that the companies have entered into an agreement granting Hasten the rights to develop and commercialize lerodalcibep in Greater China (Chinese Mainland, Hong Kong, Macau and Taiwan).

Key Points: 
  • LIB Therapeutics Inc. (“LIB”) and Hasten Biopharmaceutical Co., Ltd. (“Hasten”), today announce that the companies have entered into an agreement granting Hasten the rights to develop and commercialize lerodalcibep in Greater China (Chinese Mainland, Hong Kong, Macau and Taiwan).
  • LIB is a late-stage, biopharmaceutical company developing lerodalcibep for patients at very high and high-risk of cardiovascular disease (CVD).
  • We look forward to working with LIB to bring lerodalcibep to patients in Greater China as soon as possible.”
    Under the terms of the agreement, LIB has granted Hasten the exclusive rights to develop and commercialize lerodalcibep in Greater China.
  • A joint steering committee will be established to ensure alignment of lerodalcibep’s development in Greater China with LIB’s overall global development and commercialization strategy.

MediPharm Labs Publishes Study Investigating Medical Cannabis Impacts on Anxiety and Depression Outcomes in Fibromyalgia Patients

Retrieved on: 
Thursday, August 31, 2023

Between baseline and follow-up appointments, 75% of patients saw a significant decrease in their self-reported illness severity and the study reported reductions in depression and anxiety scores.

Key Points: 
  • Between baseline and follow-up appointments, 75% of patients saw a significant decrease in their self-reported illness severity and the study reported reductions in depression and anxiety scores.
  • The study data shows that medical cannabis may play an effective role in the management of fibromyalgia and associated symptoms of depression and anxiety.
  • Harvest Medicine Inc. ("Harvest Medicine" or "HMED") includes a medical clinic network, and is a wholly owned subsidiary of MediPharm Labs.
  • Anxiety scores were improved in 22% of those patients reporting mild-moderate severity, and in 48% of patients reporting severe anxiety.

OKYO Pharma Limited Reports Annual Results for the Twelve Months Ended March 31, 2023

Retrieved on: 
Tuesday, August 15, 2023

On May 2, 2023, we announced the initiation of our first clinical trial of OK-101 to treat DED.

Key Points: 
  • On May 2, 2023, we announced the initiation of our first clinical trial of OK-101 to treat DED.
  • For the twelve months ended 31 March 2023 OKYO reported a loss of $13.7 million compared to $6.3 million in the twelve months ended 31 March 2022.
  • Research and development (R&D) expenses increased to $6.3 million for the twelve months ended 31 March 2023 compared to $1.6 million in the twelve months ended 31 March 2022.
  • OKYO ended the period with $4.0 million cash as of 31 March 2023 as compared to $2.7 million on 31 March 2022.

Common diabetes drug metformin could protect against long COVID

Retrieved on: 
Wednesday, July 12, 2023

Of the 564 people who received metformin, 35 developed long COVID (6.3%) compared with 58 out of 562 (10.4%) who took a placebo.

Key Points: 
  • Of the 564 people who received metformin, 35 developed long COVID (6.3%) compared with 58 out of 562 (10.4%) who took a placebo.
  • This equates to a 41% lower risk of long COVID for patients who received metformin.
  • However, because relatively few people developed long COVID, large numbers of people needed to take metformin to prevent a single case of long COVID.
  • While it’s not clear how exactly metformin might work to protect against long COVID, this study offers a promising glimpse of how we might prevent it from developing in future.

Do psychedelics really work to treat depression and PTSD? Here's what the evidence says

Retrieved on: 
Wednesday, July 5, 2023

Psychedelic therapies have researchers excited because evidence suggests they might have lasting beneficial effects on factors that cause psychological distress beyond the treatment period.

Key Points: 
  • Psychedelic therapies have researchers excited because evidence suggests they might have lasting beneficial effects on factors that cause psychological distress beyond the treatment period.
  • This stands in contrast to most medications for psychological issues, which only directly help while people keep taking them regularly.

Early promise


    Early results from studies around the world have found psychedelic therapy might be effective for treating a range of psychological issues. For instance, most studies (but not all) have found patients tend to report fewer depression symptoms for periods ranging from several weeks to several months after psilocybin therapy. Similarly, studies have found reductions in PTSD symptoms three weeks after MDMA therapy.

Not so fast

    • In clinical trials, participants are often given either a medication or a placebo (inactive) drug – and it’s important they don’t know which they have been given.
    • However, due to the strong effects, it is difficult to prevent participants from knowing whether they have been given a psychedelic drug.
    • Given the publicity and excitement around psychedelic research in recent years, it is likely most participants have strong beliefs such therapies work.
    • The benefits of a psychedelic may seem even greater when they are compared to the experiences of disappointed participants.

Translating trials to practice

    • On a 2021 podcast, one clinical trial participant described how, in hindsight, the information they provided to the trial did not accurately capture the worsening of their symptoms.
    • There is also uncertainty about whether the findings from clinical trials mean treatments will work in private practice.
    • And while the safety of psychedelics within controlled contexts is often emphasised by advocates, less is known about safety of psychedelic therapy outside clinical trials.

Resolving issues

    • These issues do not mean the promising psychedelic research conducted over the past several decades is worthless.
    • Dutch researchers recently drafted a roadmap for psychedelic science with a checklist for future research to help avoid these pitfalls.